Table of Contents

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM

10-K

ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the Fiscal Year Ended May 31, 2021

2023

or


TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For The Transition Period From

To
.

COMMISSION FILE NUMBER

0-17988

NEOGEN CORPORATION

(Exact name of registrant as s

pecified
specified in its charter)

MICHIGAN

MICHIGAN

38-2367843

(State of other jurisdiction of

incorporation organization)

(I.R.S. Employer

Identification No.)

620 Lesher Place

Lansing, Michigan48912

(Address of principal executive offices, including zip code)

517-372-9200

517-372-9200

(Registrant’s telephone number, including area code)

SECURITIES REGISTERED PURSUANT TO SECTION 12(b) OF THE ACT:

Title of each Class

Trading
Symbol(s)

Trading
Symbol(s)

Name of each exchange

on which registered

Common Stock,

, $0.16 par value per share

NEOG

NEOG

NASDAQ Global Select Market

SECURITIES REGISTERED PURSUANT TO SECTION 12(g) OF THE ACT:

(Title of Class)

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes No

Indicate by a check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act.

Yes
No

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes No

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation

S-T
232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes No

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a

non-accelerated
filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer”, “accelerated filer”, “smaller reporting company” and “emerging growth company” in Rule
12b-2
of the Exchange Act.

Large accelerated filer  ☒

Accelerated filer  ☐

Non-accelerated filer  ☐

Smaller reporting company

Emerging growth company  ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Indicate by check mark whether the registrant has filed a report on and attestation to its management’s assessment of the effectiveness of its internal control over financial reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered public accounting firm that prepared or issued its audit report.

If securities are registered pursuant to Section 12(b) of the Act, whether the financial statements of the registrant included in the filing reflect the correction of an error to previously issued financial statements. ☐

Whether any of those error corrections are restatements that required a recovery analysis of incentive-based compensation received by any of the registrant's executive officers during the relevant recovery period pursuant to § 240.10D-1(b). ☐

Indicate by check mark whether the registrant is a shell company (as defined in Rule

12b-2
of the Act). Yes ☐ No

Based on the closing sale price on November 30, 20202022 the aggregate market value of the voting stock held by

non-affiliates
of the registrant was $3,951,774,000.$3,572,273,371. For these purposes, the registrant considers its Directors and executive officers to be its only affiliates.

The number of outstanding shares of the registrant’s Common Stock was 107,477,445216,308,912 on June 30, 2021.


2023.

DOCUMENTS INCORPORATED BY REFERENCE

Certain portions of the registrant’s definitive proxy statement to be prepared pursuant to Regulation 14a and filed in connection with solicitation of proxies for its October 7, 202125, 2023 annual meeting of shareholders are incorporated by reference into part III of the Form

10-K.


Table of Contents

TABLE OF CONTENTS

BUSINESS3
RISK FACTORS14

ITEM 1.

BUSINESS

3

ITEM 1A.

RISK FACTORS

15

ITEM 1B.

UNRESOLVED STAFF COMMENTS

21

30

PROPERTIES

PROPERTIES21

30

LEGAL PROCEEDINGS

22

30

MINE SAFETY DISCLOSURES

22

30

MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

22

31

[RESERVED]

SELECTED FINANCIAL DATA24

31

MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

25

32

QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKS

37

45

FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

37

45

CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE

37

45

CONTROLS AND PROCEDURES

37

45

OTHER INFORMATION

38

50

DISCLOSURE REGARDING FOREIGN JURISDICTIONS THAT PREVENT INSPECTIONS

38

50

DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE

40

51

EXECUTIVE COMPENSATION

42

53

SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT, AND RELATED STOCKHOLDER MATTERS

42

53

CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE

42

53

PRINCIPAL ACCOUNTANT FEES AND SERVICES

42

53

EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

42

54

FORM 10-K SUMMARY

FORM

10-K54 SUMMARY

42

44

F-1

Subsidiaries

Subsidiaries

Consent of independent registered public accounting firm — BDO USA, LLPP.A.

Section 302 Certification of Principal Executive Officer

Section 302 Certification of Principal Financial Officer

Section 1350 Certification pursuant to Section 906

1


Table of Contents

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING INFORMATION

Forward-looking statements, within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, are made throughout this Annual Report on Form

10-K,
including statements relating to management’s expectations regarding new product introductions; the adequacy of our sources for certain components, raw materials and finished products; and our ability to utilize certain inventory. For this purpose, any statements contained herein that are not statements of historical fact may be deemed to be forward-looking statements. Without limiting the foregoing, the words “believes,” “anticipates,” “plans,” “expects,” “seeks,” “estimates,” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are intended to provide our current expectations or forecasts of future events; are based on current estimates, projections, beliefs, and assumptions; and are not guarantees of future performance. Actual events or results may differ materially from those described in the forward-looking statements. There are a number of important factors, including circumstances beyond our control at our transition manufacturing partner, competition, recruitment, andretention, dependence on key employees, impact of weather on agriculture and food production, effects ofglobal business disruption caused by the ongoing
COVID-19
pandemic on our business, results of operations, liquidity, financial conditionRussia invasion in Ukraine and stock price,related sanctions, identification and integration of acquisitions, research and development risks, patent and trade secretintellectual property protection, government regulation and other risks detailed in item 1A. RISK FACTORS in this Form
10-K
and from time to time in the Company’s reports on file at the Securities and Exchange Commission (SEC), that could cause Neogen Corporation’s results to differ materially from those indicated by such forward-looking statements.

In addition, any forward-looking statements represent management’s views only as of the day this Annual Report on Form

10-K
was first filed with the Securities and Exchange Commission and should not be relied upon as representing management’s views as of any subsequent date. While management may elect to update forward-looking statements at some point in the future, it specifically disclaims any obligation to do so, even if its views change.

As used in this Annual Report on Form

10-K,
the terms “Neogen,” “the Company,” “we,” “us,” and “our” refer to Neogen Corporation and, where appropriate, its consolidated subsidiaries, unless the context indicates otherwise.

2


Table of Contents

PART I

ITEM 1.
BUSINESS

(Dollar amounts in thousands)

ITEM 1. BUSINESS

Neogen Corporation and its subsidiaries develop, manufacture, and market a diverse line of products and services dedicated to food and animal safety. Our Food Safety segment consists primarily of diagnostic test kits and complementary products (e.g., culture media) sold to food producers and processors to detect dangerous and/or unintended substances in human food and animal feed, such as foodborne pathogens, spoilage organisms, natural toxins, food allergens, genetic modifications, ruminant

by-products,
meat speciation, drug residues, pesticide residues and general sanitation concerns. Our diagnostic test kits are generally easier to use and provide greater accuracy and speed than conventional diagnostic methods. The majority of thethese test kits are disposable,
single-use,
immunoassay and DNA detection products that rely on proprietary antibodies and RNA and DNA testing methodologies to produce rapid and accurate test results. Our expanding line of food safety products also includes genomics-based diagnostic technology and advanced software systems that help testers to objectively analyze and store their results and perform analysis on the results from multiple locations over extended periods.

On September 1, 2022, Neogen, 3M Company (“3M”) and Neogen Food Safety Corporation (“Neogen Food Safety Corporation”), a subsidiary created to carve out 3M’s Food Safety Division (“3M FSD”, “FSD”), closed on a transaction combining 3M’s FSD with Neogen in a Reverse Morris Trust transaction and Neogen Food Safety Corporation became a wholly owned subsidiary of Neogen (“FSD transaction”, the "Transaction"). Following the FSD transaction, pre-merger Neogen Food Safety Corporation stockholders own, in the aggregate, approximately 50.1% of the issued and outstanding shares of Neogen common stock, and pre-merger Neogen shareholders own, in the aggregate, approximately 49.9% of the issued and outstanding shares of Neogen common stock. See Note 3 "Business Combinations" to the consolidated financial statements for further discussion. FSD products are reported in the Food Safety segment.

Neogen’s Animal Safety segment is engaged in the development, manufacture, marketing, and distribution of veterinary instruments, pharmaceuticals, vaccines, topicals, parasiticides, diagnostic products, rodenticides,rodent control products, cleaners, disinfectants, insecticidesinsect control products and genomics testing services for the worldwide animal safety market. The majority of these consumable products are marketed through veterinarians, retailers, livestock producers, and animal health product distributors. Our line of drug detection products is sold worldwide for the detection of abused and therapeutic drugs in animals and animal products, and has expanded into the workplace and human forensic markets.

Neogen’s products are marketed by our sales personnel in the U.S., Canada, Mexico, Central America, Brazil, Argentina, Uruguay, Chile, the United Kingdom, the European Union, China, India and Australia, and by distributors throughout the rest of the world.

Our mission is to be the leading company in the development and marketing of solutions for food and animal safety. To meet this mission, a growth strategy consisting of the following elements has been developed: (i) increasing sales of existing products; (ii) introducing innovative products and services; (iii) growing international sales; and (iv) acquiring businesses and forming strategic alliances. We have been historically been successful at increasing product sales organically, including international growth, and maintain an active acquisition program to identify and capitalize on opportunities to acquire new products, businesses or technology.

Neogen Corporation was formed as a Michigan corporation in June 1981 and operations began in 1982. Our principal executive offices are located at 620 Lesher Place, Lansing, Michigan 48912-1595, and our telephone number is

(517) 372-9200.

Neogen’s Annual Report on Form

10-K,
Quarterly Reports on Form
10-Q,
Current Reports on Form
8-K,
and amendments to those reports are available free of charge via our website (
www.neogen.com
) as soon as reasonably practicable after such information is filed with, or furnished to, the United States Securities and Exchange Commission. The content of our website or the website of any third party that may be noted herein is not incorporated by reference in this Form
10-K.

3


PRODUCTS

Product trademarks and registered trademarks owned by Neogen include:

CORPORATE:

NEOGEN
®
Neogen®, NEOGENNeogen flask (logo)
®
, NEOGENNeogen and flask (logo)
®
;
, NeoCenter™

FOOD SAFETY:

AccuClean
®
AccuClean®, AccuPoint
®
AccuPoint®, AccuScan
®
AccuScan®, Acumedia
®
Acumedia®, Agri-Screen
®
Agri-Screen®, Alert
®
Alert®, ANSR
®
ANSR® , BetaStar
®
Betastar®, BioLumix
®
BioLumix®, Ceralpha
®
Ceralpha®, Colitag
Clean-Trace®, Colitag™, F.A.S.T.
®
, GeneQuence
®
Freeze Watch®, GENE-TRAK
®
GeneQuence®, Harlequin
®
Harlequin®,
ISO-GRID
®
Iso-Grid®, Lab M
®
,
Listeria
Right Now
Now™, Megazyme
®
Megazyme®, Megazyme (design)
®
®, MonitorMark®, MPNPlate
MPNTray™, MPNTray
NeoColumn™, NeoCare
NeoNet®, NeoColumn
NeoSeek™, NeoFilm
®
NEO-GRID®, NeoNet
®
Penzyme®, NeoSeek
,
NEO-GRID
®
Petrifilm®, Penzyme
®
Raptor®, Raptor
®
Reveal®, Reveal
®
Soleris®, Soleris
®
µPREP®, µPREP
®
, Veratox
®
, Simple. Accurate. Supported. Food Safety Solutions
SM
;
Veratox®

LIFE SCIENCES:

Alert
®
,
K-Blue
®
,
K-Blue
Substrate
®
,
K-Gold
®
Alert®, NeoSal
®
;
K-Blue®, K-Gold®, NeoSal®

ANIMAL SAFETY:

Acid-A-Foam
Acid-A-Foam™, Aero-ssault
,
Ag-Tek
®
Ag-Tek®, AluShield
AluShield™, AquaPrime
®
AquaPrime®, Assault
®
Assault®, Barnstorm
®
Barnstorm®, BioCres
BioCres™ 50, BioPhene
BioPhene™, BioQuat
BioQuat™, BotVax
®
BotVax®, Breeder-Sleeve
®
Breeder-Sleeve®, Calf Eze
Eze™, Chem-Tech, Ltd.
, Chem-Tech’s CT logo (with circle)
,
Chlor-A-Foam
, COMPANION
,
CT-511
®
Chlor-A-Foam™, Cykill
COMPANION™, D3
CT-511®, Cykill™, D3™ Needles, DC&R
®
D3X™, DeciMax
®
DC&R®,
Di-Kill
®
DeciMax®, Di-Kill®, Dr. Frank’s
®
,
Dy-Fly
®
,
Dyne-O-Might
®
Frank’s®, Earth City Resources (design)
®
Dy-Fly®, ElectroJac
®
DX3™, Dyne-O-Might®, ElectroJac®, ELISA Technologies (design)
®
, EqStim
®
EqStim®, EquiSleeve
®
,
E-Z
Bond
,
E-Z
Catch
®
EquiSleeve™, Farm-Foam
E-Z Catch®, Farmphene
®
,
Final-Fly-T
®
,
Fly-Die
Defense
,
Fly-Die
Ultra
Farm-Foam™, Fura-Zone
®
Final-Fly-T®, GenQuat
Fly-Die Defense™, Fly-Die Ultra™, Fura-Zone®, Gene-Trak®, Horse Sense
®
Sense®, Ideal
®
Ideal®, ImmunoRegulin
®
ImmunoRegulin®, Insight
Iodis®, Iodis
®
Jolt®, Jolt
®
,
LD-44
®
,
LD-44T
LD-44T™, MACLEOD
®
LD-44Z™, MACLEOD®, Maxi Sleeve
®
Sleeve®, MaxKlor
®
MegaShot™, MegaShot
Viroxide Super™, MycAseptic
, NeedleGard
, NEOGEN
®
Viroxide Super
, NEOGEN
®
Neogen® Viroxide Super and flask (design)
®, NFZ
NFZ™, Nu Dyne
®
Dyne®, PanaKare
PanaKare™, Pantek
Paradefense®, ParlorMint
Parvosol®, Parvosol
®
, Peraside
Peraside™, Place Pack
®
Pack®, PolyPetite
PolyPetite™, PolyShield
PolyShield™, PolySleeve
®
PolySleeve®, Preserve
®
Preserve®, Preserve International
®
International®, Preserve International(design)
®
, Prima
®
Prima®, Prima Marc
Marc™, Prima-Shot
Prima-Shot™, Prima Tech
®
,
Pro-Fix
®
,
Pro-Flex
®
Tech®, Promar
,
Pro-Shot
,
PRO-TECT
6 MIL
®
Pro-Fix®, Prozap
®
Pro-Flex®,Pro-Shot™, Protectus™, Provecta®, Provecta Advanced®, Prozap®, Prozap (stylized mark w/fancy Z)
,
PY-75
, Ramik
®
PY-75™, Rat &
Mouse-A-Rest
II
®
,
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Table of Contents
RenaKare
Ramik®, Rodent Elimination Station
RenaKare™, Rodex
,
Rot-Not
,
Safe-T-Flex
Rodex™, Siloxycide
®
Safe-T-Flex™, Spectrasol
Siloxycide®, Spec-Tuss
Squire®, Squire
®
Standguard®, Standguard
®
Stress-Dex®, Starlicide
®
,
Stress-Dex
®
SureBond®, SureBond
®
SureKill®, SureKill
®
,
Swine-O-Dyne
®
Swine-O-Dyne®, Synergize
®
Synergize®, Tetrabase
®
Tetrabase®, Tetracid
®
Tetracid®, Tetradyne
®
Tetradyne®, ThyroKare
ThyroKare™,Tri-Hist®, TopHoof
,
Tri-Hist
®
,
Tri-Seal
Triplox™, Turbocide
®
Paradefense®, Turbocide®, Turbocide Gold
®
Gold®, Uniprim
®
Uniprim®, UriKare
VAP-5™,
VAP-5
VAP-20™,
VAP-20
Vet-Tie™,
Vet-Tie
,
Vita-15
Vita-15™, War Paint
®
,
X-185
;
GENOMICS:
Deoxi
Paint®, Envigor
X-185™

GENOMICS:Aviandx and Design®, GeneSeek

®
Canine HealthCheck®, Canine HealthCheck and Design®, CatScan and Design®, EarlyBird Sex Identification®, Envigor™, GeneSeek®, Genomic Profiler
Profiler™, Genomic Insight for Personalized Care
Care™, Igenity
®
Igenity®, SeekGain
Infiniseek™, SeekSire
Paw Print Genetics®, SeekTrace
Paw Print Pedigrees®, SeekGain™, SeekSire™, Skimseek®, Early Warning
;
Warning™

LOGOTYPES:

BioSentry barn logo
®
logo®, BioSentry chicken logo
®
logo®, BioSentry pig logo
®
logo®, Circular design
®
design®, TurboCide
®
TurboCide® (stylized), D3 color mark – red
®
.
red®

Neogen operates in two business areas: the Food Safety and the Animal Safety segments. See the “Notes to Consolidated Financial Statements” section of this Form

10-K
for financial information about our business segments and international operations.
FOOD SAFETY SEGMENT

Food Safety Segment

Neogen’s Food Safety segment primarily is primarily engaged in the production and marketing of diagnostic test kits and complementary products marketed to food and feed producers and processors to detect dangerous and/or unintended substances in food and animal feed, such as foodborne pathogens, spoilage organisms, natural toxins, food allergens, genetic modifications ruminant

by-products,
meat speciation, drug residues, pesticide residues and general sanitation concerns. Our test kits are used to detect potential hazards or unintended substances in food and animal feed by testers ranging from small local grain elevators to the largest, best-known food and feed processors in the world, and numerous regulatory agencies. Along with detection of contaminants in foods, we also detect beneficial components in foods such as dietary fiber and carbohydrates. Neogen’s products include tests for:

4


Mycotoxins.

Grain producers and processors of all types and sizes use our Veratox, Agri-Screen, Reveal, Reveal Q+ and Reveal Q+ MAX tests to detect the presence of mycotoxins, including aflatoxin, aflatoxin M1, deoxynivalenol, fumonisin, ochratoxin, zearalenone,
T-2/HT-2
toxin and ergot alkaloid, to help ensure product safety and quality in food and animal feed.

Food allergens.

The world’s largest producers of cookies, crackers, candy, ice cream and many other processedbetaprocessed foods use our Veratox, Alert, Reveal, Reveal
3-D
and BioKits testing products to help protect their food-allergic customers from the inadvertent contamination of products with food allergens, including but not limited to peanut, milk, egg, almond, gliadin (gluten), soy, hazelnut and coconut residues.
Dairy antibiotics.
Dairy processors Also included in our food allergen testing portfolio are Allergen Protein Rapid Kits and Allergen Protein ELISA Kits, acquired as part of the primary usersFSD transaction in September of Neogen’s BetaStar diagnostic tests to detect the presence of veterinary antibiotics in milk. The presence of these drugs above a certain level in milk is a public health hazard and an economic risk to producers as it limits the milk’s further processing.
2022.

Foodborne pathogens.

Meat and poultry processors, seafood processors, fruit and vegetable producers and many other market segments are the primary users of Neogen’s ANSR and Reveal tests for foodborne bacteria, including
E. coli
O157:H7,
Salmonella
,
Listeria
and
Campylobacter
. Neogen’s ANSR pathogen detection system is an isothermal amplification reaction test method whichthat exponentially amplifies the DNA of any bacteria present in food and environmental samples to detectable levels in 10 minutes. Combined with ANSR’s single enrichment step, Neogen’s pathogen detection method provides
DNA-definitive
results in a fraction of the time of other molecular detection methods. The Molecular Detection System, an isothermal DNA detection and bioluminescence device, and unique Molecular Detection Assays provide a total solution for fast and accurate pathogen detection, acquired as part of the FSD transaction in September 2022. Our
Listeria
Right Now test detects the pathogen in less than 60 minutes without sample enrichment. Reveal’s lateral flow device combines an immunoassay with chromatography for a rapid and accurate
one-step
result.

Spoilage microorganisms.

Neogen’s Soleris products are used by food processors to identify the presence of spoilage organisms (e.g., yeast and mold) and other microbiological contamination in food. The systems measure microbial growth by monitoring biochemical reactions that generate a color change in the media as microorganisms grow. The sensitivity of the system allows detection in a fraction of the time needed for traditional methods, with less labor and handling time. In July 2020, we launched Soleris NG, a next generation version of the platform, which features enhanced hardware and software for results that are easier to analyze and audit. Our NeoSeek genomics services utilize a novel application of metagenomics to determine all bacteria in a sample, without introducing biases from culture media, and without the need to generate a bacterial isolate for each possible microbe in a sample.
The Microbial Luminescence System (MLS II), acquired in the September 2022 FSD transaction, is designed for the rapid detection of microbial contamination in dairy and dairy-related products, utilizing adenosine triphosphate ("ATP") bioluminescence technology.

Sanitation monitoring.

Neogen manufactures and markets our AccuPoint Advanced rapid sanitation test to detect the presence of adenosine triphosphate (ATP),ATP, a chemical found in all living cells. This
Also included in our ATP sanitation monitoring portfolio is the Clean-Trace™ hygiene monitoring system, acquired as part of the FSD transaction in September 2022. These easy-to-use
and inexpensive test usestests use bioluminescence to quickly determine if a contact surface has been completely sanitized. When ATP comes into contact with reagents contained in the test device, a reaction takes place that produces light. More light is indicative of higher levels of ATP and a need for more thorough sanitation. In May 2021, we launched AccuPoint Advanced NG, a next generation version, designed to be simpler to use, and provide results that are easier to analyze. Our worldwide customer base for ATP sanitation testing products includes food and beverage processors, the food service and healthcare industries, as well as many other users.

Seafood contaminants.

Neogen’s specialty products for the seafood market include tests for histamine, a highly allergenic substance that occurs when certain species of fish begin to decay; and sulfite, an effective but potentially allergenic shrimp preservative; and shellfish toxins.
4

Table of Contents
Neogen’s Reveal lateral flow tests for shellfish toxins include rapid tests to detect the toxins that cause amnesic shellfish poisoning (ASP), diarrhetic shellfish poisoning (DSP) and paralytic shellfish poisoning (PSP).
preservative.

Waterborne microorganisms.

Neogen offers the food and beverage industries, including water companies, several platforms for performing the microbial analysis of water. This includes Neogen’s filter tests, which are a combination of Neogen Filter membrane filtration and Neogen Culture Media ampouled media, and
an easy-to-use
Colitag product. With Colitag, after an incubation period, the sample changes color in the presence of coliforms and fluoresces in the presence of
E. coli
.

5


Culture media.

Neogen Culture Media, formerly Neogen’s Acumedia and Lab M products, offers culture media and prepared media for varied purposes, including traditional bacterial testing and the growth of beneficial bacteria, such as cultures for sausages and beer. Also included under Neogen Culture Media is the Petrifilm solution, acquired as part of the FSD transaction in September 2022. Petrifilm standard and rapid plates are all-in-one plating systems that serve as an efficient method for the detection and enumeration of various microorganisms. Our customers for culture media also include commercial and research laboratories and producers of pharmaceuticals, cosmetics and veterinary vaccines.

Food quality diagnostics.

Through the December 2020 acquisition of Ireland-based Megazyme, Ltd., Neogen supplies diagnostic kits and specialty enzymes used worldwide by quality control laboratories in the food, animal feed and beverage industries. Megazyme’s validated assays and reagents are used across various food industries such as the grain, wine and dairy markets, to measure dietary fibers, complex carbohydrates, simple sugars and organic acids, such as lactose.

Sample handling. Neogen offers a range of sample handling products, acquired through the September 2022 FSD transaction. These innovative solutions are designed to make environmental and carcass sample collection and preparation more reliable and convenient than traditional methods. These products are manufactured to meet the highest quality standards and government regulations, maximizing accuracy, consistency and efficiency, while remaining cost efficient.

Digital services.

Our new food safety and risk management software as a service,software-as-a-service, Neogen Analytics, delivers a comprehensive Environmental Monitoring Program (EMP) automation solution for food companies. The software reduces risk by increasing the visibility toof food safety testing results, elevating the ability to enforcecomply with and improve food safety standards. Neogen Analytics builds upon innovative technologies like our AccuPoint Advanced Next GenerationWith the Corvium acquisition in February 2023, Neogen's capabilities expanded with additional services and ANSR systems, offering floor plan mapping, smart test scheduling, easily filteredmodules to include data aggregation and auditable data management,digitalized workflow services for product testing and corrective actions.
sanitation programs.

Laboratory services.

Neogen offers food safety analysis services in the United States ("U.S."), United Kingdom (U.K.("U.K.") and India. These
ISO-accredited
laboratories offer a variety of
fee-for-service
tests for the food and feed industry.
industries.

The majority of Neogen’s food safety test kits use immunoassay technology to rapidly detect target substances. Our ability to produce high qualityhigh-quality antibodies sets our products apart from immunoassay test kits produced and sold by other companies. Our kits are available in microwell formats, which allow for automated and rapid processing of a large number of samples, andas well as lateral flow and other similar devices that provide distinct visual results. Typically, test kits use antibody-coated test devices and chemical reagents to indicate a positive or negative result for the presence of a target substance in a test sample; thesample. The simplicity of the tests makes them accessible to all levels of food producers, processors and handlers. Neogen also offers other testtesting methods and products to complement its immunoassay tests.

Our test kits are generally based on internally developed technology, licensed technology, or technology that is acquired in connection withas a result of acquisitions. In fiscal 2021,2023, the Food Safety segment incurred expense totaling $1,798,000$3,118 for royalties for licensed technology used in our products, including expense of $856,000$838 for allergen products and $411,000$489 for the pathogen product line. Generally, royalty rates are in the range of 2% to 10% of revenues on products containing the licensed technology. Some licenses involve technology that is exclusive to Neogen’s use, while others are

non-exclusive
and involve technology licensed to multiple licensees.

Neogen’s international operations in the U.K., Europe, Mexico, Guatemala, Brazil, Argentina, Uruguay, Chile, China and India originally focused on food safety products, and each of these units reports through the Food Safety segment. In recent years, these operations have expanded to offer our complete line of products and services, including those usually associated with the Animal Safety segment, such as cleaners, disinfectants, rodenticides, insecticides,rodent control, insect control, veterinary instruments and genomics services. These additional products and services are managed and directed by existing management at our international operations and report through the Food Safety segment.

Revenues from Neogen’s Food Safety segment accounted for 50.0%66.5%, 50.9%49.3%, and 51.5%50.0% of our total revenues for fiscal years ended May 31, 2023, 2022 and 2021, 2020 and 2019, respectively.

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ANIMAL SAFETY SEGMENT

Neogen’s Animal Safety segment is primarily engaged in the development, manufacture, marketing, and distribution of veterinary instruments, pharmaceuticals, vaccines, topicals, parasiticides, diagnostic products, a full suite of agricultural biosecurity products such as rodenticides,rodent control, cleaners, disinfectants and insecticides,insect control, and genomics services.

Veterinary instruments.

Neogen markets a broad line of veterinary instruments and animal health delivery systems primarily under the Ideal brand name. Approximately 250 different products are offered, many of which are used to deliver animal health products, such as antibiotics and vaccines. Ideal’s D3 and D3X Needles are stronger than conventional veterinary needles and are uniquely detectable by metal detectors at meat processing facilities — a potential market advantage in the safety-conscious beef and swine industries. Neogen’s Prima Tech product line consists of highly accurate devices used by farmers, ranchers and veterinarians to inject animals, provide topical applications and to use for oral administration. The Prima Tech isline also a supplier ofincludes products used in artificial insemination in the swine industry. Other products includeindustry, animal identification products and handling equipment.
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Table of Contents

Veterinary pharmaceuticals.

Animal Safety’s NeogenVet product line provides innovative, value-added, high quality products to the veterinary market. Top NeogenVet products include PanaKare, a digestive aid that serves as a replacement therapy where digestion of protein, carbohydrate and fat is inadequate due to exocrine pancreatic insufficiency; Natural Vitamin
E-AD,
which aids in the prevention and treatment of vitamin deficiencies in swine, cattle and sheep; RenaKare, a supplement for potassium deficiency in cats and dogs; and ThryroKare,ThyroKare, a supplement used as replacement therapy for dogs with diminished thyroid function. Other products sold under the NeogenVet brand include
Vita-15
and Liver 7, which are used in the treatment and prevention of nutritional deficiencies. WeNeogen also manufacture and marketmarkets Uniprim, a veterinary antibiotic.
antibiotic, and several companion animal parasiticides.

Veterinary biologics.

Neogen’s BotVax B vaccine has successfully protected thousands of horses and foals against Type B botulism, commonly known as Shaker Foal Syndrome. Our product is the only USDA-approved vaccine for the prevention of Type B botulism in horses. Years of research and many thousands of doses have proven Neogen’s EqStim immunostimulant to be safe and effective as a veterinarian-administered adjunct to conventional treatment of equine bacterial and viral respiratory infections. OurThe Company’s ImmunoRegulin product uses similar immunostimulant technology to aid in the treatment of pyoderma (a bacterial skin inflammation) in dogs.

Veterinary OTC products.

Animal Safety products offered by Neogen to the retail
over-the-counter
(OTC) market include Ideal brand veterinary instruments packaged for the retail market. OTC products also include
Stress-Dex,
an oral electrolyte replacer for performance horses, and Fura-Zone, for the prevention and treatment of surface bacterial infections in wounds, burns and cutaneous ulcers. Hoof care, disposables and artificial insemination supplies are marketed to the dairy and veterinary industries.
Rodenticides.

Rodent control products.Neogen’s comprehensive line of proven rodenticides,rodent control products, sold under brand names such as Ramik, CyKill and Havoc, effectively address rodent problems of any size and serve as a critical component of an overall biosecurity plan for animal protein production operations. Neogen offers several rodenticide active ingredients, including diphacinone, bromethalin, brodifacoum and zinc phosphide, formulated with food gradefood-grade ingredients to generate the highest acceptance and most palatable bait possible.

Cleaners and disinfectants.

Used in animal and food production facilities, Neogen’s cleaners and disinfectants, including Synergize, 904 Disinfectant,
Acid-A-Foam,
Synergize, BioPhene, Neogen Viroxide Super, and Companion, can stop aprevent disease outbreak before it starts.outbreaks. The products are also used in the veterinary clinic market to maintain sanitary conditions and limit the potential hazards of bacteria, fungi and viruses. Neogen’s water line cleaner and disinfectant products, including Peraside, NeoKlor, AquaPrime and Siloxycide, are used to clean water lines and provide continuous disinfection of a livestock facility’s water supply.
Insecticides.

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Insect control products.Neogen’s highly effective insecticidesinsect control products utilize environmentally friendly technical formulas, and several are approved for use in food establishments and by pest control professionals in a wide range of environments. The Company’s Prozap insecticideinsect control brand is used in the large animal production industry, particularly with dairy and equine producers. Neogen’s SureKill line of products is used by professionals to control a variety of insects, and the Company’s StandGuard

Pour-on
solution acquired in July 2020, is used for horn fly and lice control in beef cattle.

Animal genomics services.

Neogen Genomics formerly known as GeneSeek, provides value-added services to leading agricultural genetics providers, large national cattle associations, companion animal breed registries and direct to consumerdirect-to-consumer canine genetic test providers, university researchers, and numerous commercial beef and dairy cattle, swine, sheep and poultry producers. With
state-of-the-art
genomics laboratories and the comprehensive bioinformatics to interpret genomics test results, Neogen Genomics offers identity and trait determination and analysis. Our technology employs high-density DNA genotyping and genomic sequencing for identity and trait analysis in a variety of important animal and agricultural plant species. Our extensive bioinformatics database identifies and predicts an animal’s positive or negative traits based on DNA test results. This information has helped livestock producers increase the speed of genetic improvement in their herds and the overall performance and quality of their animals.
Neogen’s December 2021 acquisition of Genetic Veterinary Sciences, Inc. expanded the Company’s portfolio through the addition of a number of genetic tests for companion animals, including dogs, cats and birds.

Life sciences.

Neogen’s Life Science/Toxicology line of approximately 100products include reagents and test kits for immunoassay production, life science research, and forensic and animal toxicology. Product offering includes a wide range of tests to provide solutions for drugs of abuse, including designer drugs and emerging drugs. The drug detection immunoassayassays include over 100 test kits is sold worldwideused to screen more than 300 drugs and their metabolites in various forensic matrices, including oral fluid, whole blood, urine, serum, plasma, meconium, and others. Our portfolio for the detectionlife science research includes assays for detecting levels of approximately 300 abusedhormones, steroids, lipoxins, and therapeutic drugshistamine in farm animalsa wide range of samples and racing animals,species types. Additionally, we offer reagents and unique colorimetric and chemiluminescent substrates for the detection of drug residues in meatimmunoassay production and meat products. The test kits are also used for human forensic toxicology drug screeningresearch applications. This line includes tests for narcotics, analgesics, stimulants, depressants, tranquilizers, anesthetics, steroids and diuretics. Neogen also has several products used by researchers for the detection of biologically active substances.

Many of the products and services in the Animal Safety segment use licensed technology. In fiscal year 2021,2023, the Animal Safety segment incurred expense totaling $331,000$274 for royalties for licensed technology used in our products and services, including expense of $213,000$152 related to the genomics services line.

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services.

Neogen’s operation in Australia originally focused on providing genomics services and sales of animal safety products and reports through the Animal Safety segment. With the acquisition of Cell BioSciences in February 2020, our Australian operationIt has expanded to offer our complete line of products and services, including those usually associated with the Food Safety segment. These additional products are managed and directed by existing management at Neogen Australasia and report through the Animal Safety segment.

Revenues from Neogen’s Animal Safety segment accounted for 50.0%33.5%, 49.1%50.7%, and 48.5%50.0% of our total revenues for fiscal years ended May 31, 2023, 2022 and 2021, 2020 and 2019, respectively.

GENERAL SALES AND MARKETING

Neogen is organized under two segments — Food Safety and Animal Safety. Within these segments, our sales efforts are generally organized by specific markets, and/or geography. During the fiscal year that ended May 31, 2021,2023, we had approximately 33,00041,000 customers for our products. As many of our customers are distributors and certain animal safety products are offered to the general retail market, the total number of end users of our products is considerably greater than 33,000.41,000. As of May 31, 2021,2023, a total of 494904 employees were assigned to sales and marketing functions, compared to 507573 at the end of May 2020.2022. During the fiscal years ended May 31, 2021, 20202023, 2022 and 2019,2021, no single customer or distributor accounted for 10% or more of our revenues.

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DOMESTIC SALES AND MARKETING

FOOD SAFETY

To reach each customer and prospect with expertise and experience, Neogen has a staff of specialized food safety sales and technical service representatives assigned to specific markets or geographies. This staff sells our products directly to end users and also handles technical support issues that arise with customers in the United States.

customers.

Neogen’s food safety markets are primarily comprised of:

Milling and grain
, including grain elevators, feed mills, pet food manufacturers and grain inspection companies;
Meat and poultry
, including meat and poultry processors, producers of
ready-to-eat
meat and poultry products, and the USDA’s Food Safety Inspection Service (FSIS);
Prepared foods and ingredients
, including flour millers, malters, bakeries, candy and confection manufacturers, manufacturers of prepared meals, nuts, spices, cookies, crackers and other snack foods;
Fruits and vegetables
, including growers and processors of juice and packaged fresh cut grocery items;
Seafood
, including harvesters and processors of a wide variety of seafood products;
Dairy
, including milk and yogurt processors;
Beverage
, including soft drink bottlers and beer and wine producers;
Water,
including food producers, water bottlers and municipal water departments;
Healthcare
, including hospitals and distributors to the healthcare industry;
Traditional culture media markets
, including commercial and research laboratories and producers of pharmaceuticals, cosmetics and veterinary vaccines;
Food service
, including fast food service establishments and retail grocery market chains; and
Dietary supplements
, including producers and marketers of a wide variety of nutritional and holistic consumer products.

ANIMAL SAFETY

Neogen’s staff of specialized animal safety sales, marketing, customer and technical service representatives sell our products and services directly to consumers, dealers, veterinarians, distributors and other manufacturers and also handle domestic technical support issues. Neogen further supports its distribution channels through product training, field support, various promotions and advertising.

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Neogen’s animal safety markets are primarily comprised of:

Companion animal veterinarians.
Neogen has a dedicated sales group that sells and technically supports the Company’s animal care, biosecurity and disposable products to the companion animal veterinary market.veterinarians;
Livestock producers, veterinarians and breed associations.
Neogen has a dedicated group of sales professionals that sells the Company’s comprehensive suite of biosecurity and husbandry products and genomics services directly to livestock producers, and livestock veterinarians and veterinary clinics.associations;
Retailers,including large farm and ranch retailers;
Distributors.Breeding and genetics companies, including large dairy artificial insemination providers, poultry and swine genetics companies and the aquaculture industry;
Diagnostic labs and universities,including commercial and forensic testing laboratories;
Distributors. To expand the reach of its animal safety OTC and veterinary products, Neogen has a dedicated sales team that sells the Company’s products to animal health product distributors.distributors;
Retailers.
Neogen offers select animal care and biosecurity products directly to large farm and ranch retailers for sale to consumers.
Breeding and genetics companies.
Neogen has sales professionals who sell directly to the large dairy artificial insemination providers, poultry and swine genetics companies and the aquaculture industry.
Diagnostic labs and universities.
Neogen has a dedicated lab, manufacturing, sales and technical service group that calls on large commercial and forensic testing laboratories and universities.
Other manufacturers and government agencies.
Neogen has an experienced group of professionals who work directly with other manufacturers and government agencies to provide custom solution products and services for their needs.

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INTERNATIONAL SALES AND MARKETING

Neogen maintains 16 Company-owned locations outside of the United States in 23 countries to provide a direct presence in regions of particular importance to us; wesales presence. We also maintain an extensivea network of distributors to reach countries where we do not have a direct presence.

Neogen

UK, Europe, Middle East, Africa and subsidiaries.

India.Neogen Europe, Ltd., headquartered in Ayr, Scotland, sells products and services to our network of customers and distributors throughout the United Kingdom (U.K.)U.K., Europe, the Middle East and Africa. Customers in the U.K., France, Germany, Italy, and the Netherlands, United Arab Emirates (U.A.E.) and India are served by our employees. In other regions, customers generally are generally servicedserved by distributors managed by Neogen Europe personnel.

Neogen Europe management also is also responsible for Neogen’svarious other Europeanmanufacturing operations which include:

and service providers, including Quat-Chem, Ltd., a Rochdale, England-based chemical company that specializes in the development, manufacture and sale of agricultural, industrial, and food processing biocidal hygiene products, including cleaners and disinfectants. Quat-Chem sells its products on a global basis, with a focus on markets in the U.K., Europe, Middle East, Africa and Asia.
Neogen Italia, a Milan, Italy-based business, which directly markets and sells Neogen’s products in Italy.
Megazyme, Ltd., a Bray, Ireland-based food quality diagnostics company, acquired in December 2020, which developsDelf, Ltd., and refines the analytical methods used to measure the carbohydrates and enzymes in food and feed products that affect quality.
Abbott Analytical, Ltd. Neogen Europe has two additional manufacturing locations in:
in Heywood and Liverpool, England, which manufactures an extensive range of microbiological culture media, supplements and immunomagnetic separation techniques.
Liverpool, England, a developer and supplier ofmanufacture culture media supplements and microbiology technologies.

Neogen Latinoam

é
rica.
Neogen Latinoamérica is headquartered near Mexico City and distributes Neogen’s products throughout Mexico and Central America. Neogen Latinoamérica manages our business activities throughout the region by marketing to animal and crop producers and food processors, utilizing our direct sales representatives to sell Food Safety products and genomics services, while marketing cleaners, disinfectants and other Animal Safety products primarily through distributors.
Neogen Argentina, Neogen Uruguay and Neogen Chile.
In January 2020, Neogen acquired Productos Quimicos Magiar and Lakenord S.A. (Magiar Uruguay), distributors of Neogen’s food safety diagnostics products for the past 20 years, with operations in Argentina and Uruguay, respectively. In March 2020, Neogen acquired the assets of Chile-based Magiar Chilena, a distributor of food, animal, and plant diagnostics, including Neogen products. With the acquisitions, the former Magiar operations remain in the three countries and provide Neogen with a physical presence in the important agricultural Southern Cone region of South America, which has large beef and dairy populations with significant export markets. The operations are managed through Neogen’s Latin American operations and offer direct sales of Neogen food safety, animal safety and genomics products into Argentina, Uruguay and Chile.
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Neogen do Brasil.
Neogen do Brasil, headquartered near São Paulo, distributes Neogen’s products throughout Brazil. Brazil is a world leader in the export of numerous food commodities, including beef, poultry, soybeans, coffee, corn, sugar and orange juice, and this operation gives us direct sales representation to these important markets. Neogen do Brasil management is also responsible for manufacturing, marketing and sales for Rogama, located in Pindamonhangaba, Brazil. This company operates a genomics testing laboratory (formerly named Deoxi) and develops, manufactures and markets rodenticides and insecticides. Rogama offers more than 70 registered pest control products to Brazil’s agronomic, professional and retail markets.
Neogen China.
Our Chinese subsidiary, located in Shanghai, employs sales representatives who sell directly to Chinese customers. China’s burgeoning middle class, with its rapidly growing demand for higher quality meat and dairy products, makes the country a growth opportunity for Neogen’s products and services — both for animal production on the country’s farms, and in processing plants throughout China’s food production and distribution channels. The business also operates a genomics testing laboratory. We utilize both direct sales representatives and distributors to sell our complete portfolio in this growing market.
Neogen India.
This business operates an accredited laboratory whichin India, located in Kochi, in the state of Kerala, that performs food safety and water quality testing for food producers, major hotels and restaurants in its home region, as well as safety and quality analysis for the country’s expanding nutraceutical market, and growing food export businesses. The laboratory is located

Mexico, Central and South America. Neogen maintains offices and distribution facilities in Kochi, inMexico, Guatemala, Brazil, Argentina, Chile, Uruguay and Colombia. Combined, the state of Kerala, which is India’s leading region for the export of spices, tea,businesses distribute Neogen’s products and fresh fruitsoffer genomics services throughout Mexico, Central and vegetables. South America to distributors and end customers.

Neogen Indiado Brasil, headquartered near São Paulo, is also responsible for manufacturing, marketing and sales of our food safetyfor Rogama, located in Pindamonhangaba, Brazil. This company operates a genomics testing laboratory (formerly named Deoxi) and animal safetydevelops, manufactures and markets rodent control and insect control products. Rogama offers registered pest control products to customersBrazil’s agronomic, professional and retail markets.

Asia Pacific. Neogen maintains offices in Japan, Korea, Thailand, China, Australia and New Zealand. Combined, the businesses distribute Neogen’s products throughout the Asia Pacific region to distributors and end customers.

Our Chinese subsidiary, located in India and nearby countries.

Neogen Australasia.
Neogen AustralasiaShanghai, also operates a genomics testing laboratory, focusing on theswine, dairy and beef cattle markets. Neogen’s Australasia subsidiary also operates a genomics testing laboratory, focusing on sheep and cattle markets in Australia and New Zealand, and also directly markets and sells our food and animal safety products in those countries.
Zealand.

Neogen Canada.

This business operates a genomics testing laboratory in Edmonton, Alberta.

Other distributor partners.

Outside of our physical locations, Neogen uses our own sales managers in both the Food Safety and Animal Safety segments to work closely with and coordinate the efforts of a network of approximately 400800 distributors in more than 100 countries. The distributors provide local training and technical support, perform market research and promote Company products within designated countries around the world.

Sales to customers outside the United States accounted for 39.1%48.4%, 39.4%39.7%, and 40.1%39.1% of our total revenues for fiscal years ended May 31, 2021, 20202023, 2022 and 2019,2021, respectively. No individual foreign country contributed 10% or more of our revenues for those same periods.

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RESEARCH AND DEVELOPMENT

Management maintains

Neogen has a strong commitment to Neogen’sits research and development activities. Our product development efforts are focused on the enhancement of existing products and on the development of new products that fitadvance our business strategy. As of May 31, 2021,2023, we employed 112136 scientists and support staff in our worldwide research and development group, including immunologists, chemists and microbiologists. Research and development costs were approximately $16.3 million, $14.8 million,$26,039, $17,049, and $12.8 million$16,247 representing 3.5%3.2%, 3.5%3.2%, and 3.1%3.5% of total revenues in fiscal years 2021, 20202023, 2022 and 2019,2021, respectively. Management currently expects our future research and development expenditures to approximate 3% to 4% of total revenues annually.

Neogen has ongoing development projects for several new and improved diagnostic tests and other complementary products for both the Food Safety and Animal Safety markets. Management expects that a number of these products will be commercially available at various times during fiscal years 20222024 and 2023.

2025.

Certain technologies used in some products manufactured and marketed by Neogen were acquired from or developed in collaboration with affiliated partners, independent scientists, governmental agencies, universities and other third parties. We have entered into agreements with these parties that provide for the payment of royalties based uponon sales of products that use the pertinent licensed technology. Royalties, expensed to sales and marketing, under these agreements amounted to $2,129,000, $2,524,000,$3,392, $1,999, and $2,795,000$2,129 in fiscal years 2023, 2022, and 2021, 2020 and 2019, respectively.

PROPRIETARY PROTECTION AND APPROVALS

Neogen uses a variety of intellectual property approaches to protect the competitive position of its offerings, including the use of patents, trademarks, trade secrets, proprietary and confidential know-how, as proprietary protection in many of its foodwell as branding and animal safety products. In many cases, we have developed unique antibodies capable of detecting microorganisms and residues at minute levels. The supply of these antibodies, and the proprietary techniques utilized for their development, may offer better protection than filing patents. Such proprietary reagents are maintained in secure facilities and stored in more than one location to reduce exposure to complete destruction by natural disaster or other means.

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trademarks. Patent and trademark registration applications are submitted whenever appropriate. SinceFrom its inception, Neogen has acquired and been granted numerous patents and trademarks,trademark registrations and has numerous pending patents and trademark applications. TheNeogen’s patent portfolio includes at least 48 U.S. patents, expire at various times over404 patents in countries outside of the next 21 years.
A summaryU.S., and 209 pending patent applications globally. Neogen’s trademark estate includes 119 trademark registrations within the U.S., and 548 trademark registrations in countries outside of patents by product categories follows:
   
USA
   
International
   
Expiration
 
Natural Toxins, Allergens, & Drug Residues
   19    36    2021-2042 
Bacterial & General Sanitation
   1    0    2022 
Life Sciences
   0    3    2024 
Vaccine
   1    0    2028 
Veterinary Instruments & Other
   11    33    2021-2042 
Genomics Services
   18    4    2021-2029 
the U.S, and 24 trademark registration applications globally.

We do not expect the near-term expiration of any single patent to have a significant effect on future results of operations.

Our offerings also are protected by trade secrets and proprietary know-how when appropriate. For example, many of our products employ unique antibodies capable of detecting microorganisms and other substances at minute levels. In some instances, we have chosen to keep confidential the methods and techniques used to manufacture and use those antibodies when trade secret and/or proprietary know-how protections are more appropriate.

Management believes that Neogen has adequate rights to commercialize our products. However, we are aware that substantial research is conducted at universities, governmental agencies and other companies throughout the world, and that it always is always possible that patents have been applied for and could be granted that are relevant to technologies that may be used in our products. To the extent some of our products may now, or in the future, embody technologies protected by patents or trade secrets of others, we may need to obtain licenses to use such technologies to continue to sell the products. These licenses may not be available on commercially reasonable terms. Failure to obtain any such licenses could delay or prevent the sale of certain new or existing products. In addition, patent litigation is not uncommon. Accordingly, there can be no assurance that we will continue to have adequate rights to commercialize our new products or that we will avoid litigation.

One of the major areas affecting the success of biotechnology and pharmaceutical development involves the time, cost and uncertainty surrounding regulatory approvals. Neogen products requiring regulatory approval, which we currently have in place, include BotVax B, EqStim, ImmunoRegulin Uniprim and BetaStar. Our general strategy is to focus on technical and proprietary products that do not require mandatory approval by regulatory bodies to be marketed.Uniprim. Neogen’s rodenticide, disinfectant, parasiticide and insecticide products are subject to registration in the United States and internationally.

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Neogen utilizes third-party validations and certifications on many of our disposable test kitsproducts and associated methods to provide our customers with assurancesconfidence that our products perform to specified levels. These include validation by, among others, the AOAC International, independently administered third-party, multi-laboratory collaborative studies, and approvals by the USDA Food Safety Inspection Service for the use of ourService.

PRODUCTION AND SUPPLY

Neogen manufactures products in their operations.

PRODUCTION AND SUPPLY
Neogen manufactures our products in Michigan, Kentucky, Wisconsin, North Carolina, Iowa, Tennessee, California,the U.S., the U.K., Ireland the United Kingdom and Brazil and provides genomics services in Nebraska,the U.S., Scotland, Brazil, Australia, China and Canada. As of May 31, 2021,2023, there were approximately 9201,168 full-time employees assigned to manufacturing operations and providing of services in these locations, operating on multiple shift schedules;schedules, with occasional 24/7 production during high demandhigh-demand periods. Future demand increases could be accommodated by adding shifts. Management believes we could increase the current output of our primary product lines by more than 30% using the current space available; however,available. However, to do so would require investment in additional equipment.

Food safety diagnostics.

Manufacturing of diagnostic tests for the detection of natural toxins, pathogens, food allergens dairy antibiotics,and spoilage organisms, and pesticides, final kit assembly, quality assurance and shipping takes place at our facilities in Lansing, Michigan. Proprietary monoclonal and polyclonal antibodies for Neogen’s diagnostic kits are produced on a regular schedule in our immunology laboratories in Lansing. Generally, the final assembly and shipment of diagnostic test kits to customers in Europe is performed in our Ayr, Scotland facility. MostMany of the Company’s food safety diagnostic instruments and readers are produced by third-party vendors to our specifications, quality tested in Lansing, and then shipped to customers. Culture media products are manufactured in an
ISO-approved
facility in Lansing and in Heywood and Liverpool, England. Products are blended following strict formulations or custom blended to customer specifications and shipped directly to customers from Lansing and the United Kingdom.U.K. The Heywood location produces prepared media plates, sterile liquid media, and other related products in ready to useready-to-use format for food testing laboratories across the U.K. and westernWestern Europe. Enzyme substrates are manufactured at Megazyme in Bray, Ireland.
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Our Clean-Trace product line is manufactured in Wales. Other FSD products are currently manufactured within 3M plants in the U.S. and Poland.

Animal health products.

Manufacturing of animal health products, pharmacological diagnostic test kits, and test kits for drug residues takes place in our
FDA-registered
facilities in Lexington, Kentucky. In general, manufacturing operations including reagent manufacturing, quality assurance, final kit assembly and packaging are performed by Neogen personnel. Certain animal health products and veterinary instruments that are purchased finished or that are toll manufactured by third partythird-party vendors are warehoused and shipped from our LexingtonKentucky facilities. OtherSome veterinary instruments are produced in our facilities in Lansing and are generally then shipped to LexingtonKentucky for distribution to customers. Manufacturing and shipment of devices used for animal injections, topical applications and oral administration occurs in Kenansville, North Carolina.

Veterinary biologics.

Neogen maintains a Lansing-based USDA-approved manufacturing facility devoted to the production of the biologic products EqStim and ImmunoRegulin.
P.acnes
seed cultures are added to media and then subjected to several stages of further processing resulting in a finished product that is filled and packaged within the facility. Our BotVax B vaccine also is also produced in the Lansing facility utilizingusing Type B botulism seed cultures and a traditional fermentation process. All completed biologic products are then shipped to Neogen’s Lexington facilities, where they are inventoried prior to distribution to customers.

Agricultural genomics services.

Neogen offers agricultural genomics laboratory services and bioinformatics at our locations in Nebraska,the U.S., Scotland, Brazil, Australia, China and Canada. Through our laboratory services and bioinformatics (primarily in beef and dairy cattle, pigs, sheep, poultry, horses and dogs), Neogen Genomics allows our customers to speed genetic improvement efforts, as well as identify economically important diseases.

Cleaners, disinfectants and rodenticides.

rodent control products.Manufacturing of rodenticidesrodent control products and/or cleaners and disinfectants takes place in the following locations: Randolph, Wisconsin; Memphis, Tennessee; Turlock, California; Rochdale, England;Wisconsin, Tennessee, California, England and Pindamonhangaba, Brazil. Manufacturing of rodenticidesrodent control products consists of blending technical material (active ingredient) with bait consisting principally of various grains. Certain cleaners and disinfectants are manufactured in Neogen facilities, while others are purchased from other manufacturers for resale or toll manufactured by third parties.
Insecticides.

Insect control products.Neogen manufactures insecticides and other pesticidesinsect control products at its facilities in Pleasantville, Iowa and Pindamonhangaba, Brazil.

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Neogen purchases component parts and raw materials from more than 1,000 suppliers. Though many of these items are purchased from a single source to achieve the greatest volume discounts, we believe we have identified acceptable alternative suppliers for most of our key components and raw materials where it is economically feasible to do so. There can be no assurance that we would avoid a disruption of supply in the event a supplier discontinues shipment of product. Shipments of higher volume products are generally accomplished within a

48-hour
turnaround time. Our backlog of unshipped orders at any given time has historically not been significant.

COMPETITION

Although competitors vary in individual markets, management knows of no single competitor that is pursuing Neogen’s fundamental strategy of developing and marketing a broad line of products, ranging from disposable tests and culture media to veterinary pharmaceuticals and instruments for a large number of food safety and animal safety concerns. For each of our individual products or product lines, we face intense competition from companies ranging from small businesses to divisions of large multinational companies. Some of these organizations have substantially greater financial resources than Neogen. We compete primarily on the basis of ease of use, speed, accuracy and other similar performance characteristics of our products. The breadth of our product line, the effectiveness of our sales and customer service organizations, and pricing also are also components in management’s competitive strategy.

Future competition may become even more intense and could result from the development of new technologies, which could affect the marketability and profitability of Neogen’s products. Our competitive position will also dependdepends on our ability to continue to develop proprietary products, attract and retain qualified scientific and other personnel, develop and implement production and marketing plans and obtain patent protectionprotect the intellectual property for new products. Additionally, we must continue to generate or have access to adequate capital resources to execute our strategy.

FOOD SAFETY:

With a large professional sales organization offering a comprehensive catalog of food safety solutions, management believes we maintain a general advantage over competitors offering only limited product lines. In most cases, Neogen sales and technical service personnel can offer unique insight into a customer’s numerous safety and quality challenges, and offer testing and other solutions to help the customer overcome those challenges.

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Competition for pathogen detection products includes traditional methods and antibody and genetic-based platforms; competition for natural toxins and allergen detection products includeincludes instrumentation and antibody-based tests. While our offerings will not always compete on all platforms in all markets, the products we offer provide tests that can be utilized by most customers to meet their testing needs.

In addition to our extensive product offerings and robust distribution network, we focus our competitive advantage in the areas of customer service, product performance, speed, and ease of use of our products. Additionally, by aggressively maintaining Neogen’s ability to produce at low cost, we believe that we can be competitive with new market entrants that may choose a low pricing strategy in an attempt to gain market share.

ANIMAL SAFETY:

Neogen’s Animal Safety segment faces no single competitor across the products and markets we serve. In the racing industry market, we believe we hold a leading market share position. In the life sciences and forensicstoxicology markets, we compete against several other diagnostic and reagent companies with similar product offerings.

In the veterinary market, Neogen markets BotVax B, the only USDA-approved vaccine for the prevention of botulism Type B in horses. We compete on other key products through differentiated product performance and superior customer and technical support. With some of our products, we provide solutions as a lower cost alternative and also offer a private label option for our distributors.

customers.

Competition in the rodenticiderodent control market includes several companies of comparable size that offer products into similar market segments. The retail rodenticiderodent control market is not dominated by a single brand. While the technical

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materials used by competing companies are similar, Neogen uses manufacturing and bait formula techniques, which we believe may better attract rodents to the product and thereby improves overall product performance.

Within the insecticideinsect control market, Chem-Tech products specifically focus on the area of insect control for food and animal safety applications. There are several competitors offering similar products, however, we have a proprietary formulation chemistry that optimizes the delivery and safe application of insecticidesinsect control products at the customer’s location. These products currently are currently only sold in the U.S. through a combination of direct sales and distributors.

Numerous companies, including a number of large multinationals, compete for sales in the cleaner and disinfectant product segment. Neogen’s broad line of products areis sold through our distributor network around the world, primarily to assist in the cleaning and disinfecting of animal production facilities.

In addition to our extensive portfolio of Animal Safetyanimal safety products, Neogen also competes in the retail market by providing solutions to common retail problems, such as stock outs, wasted floor space, and inconsistent brand identity. We differentiate ourselves by offering planograms and convenient reordering systems to maximize turns and profitability for our retail customers.

Neogen Genomics, thea leading worldwide commercial agriculturalanimal genomics laboratory, in the U.S., employs cutting-edge technology in the area of genomics. The result of this technology allows the acceleration of natural selection through parentage testing and selective breeding of traits such as disease resistance, yield improvement and meat quality. Competition comes mainly from a number of service providers, some significantly larger than us as well as several smaller companies offering genomics services. Neogen Genomics is not involved in cloning or the development of transgenic animals.

GOVERNMENT REGULATION

A significant portion of Neogen’s products and revenues are affected by the regulations of various domestic and foreign government agencies, including the U.S. Department of Agriculture (USDA), the Environmental Protection Agency (EPA), and the U.S. Food and Drug Administration (FDA). Changes in these regulations could affect revenues and/or costs of production and distribution.

Neogen’s development and manufacturing processes involve the use of certain hazardous materials, chemicals, and compounds. Management believes that our safety procedures for handling and disposing of such commodities comply with the standards prescribed by federal, state and local regulations; however,regulations. However, changes in such regulations or rules could involve significant costs to us and could be materially adverse to our business.

The rodenticides, insecticides,rodent control products, insect control products, cleaners, disinfectants and sanitizers manufactured and distributed by Neogen are subject to EPA and various U.S. state regulations.regulations as well as other analogous agencies in the markets where we sell such products. In general, any international sale of our products also must also comply with similar regulatory requirements in the country of destination. Each country has its own individual regulatory construct with specific requirements (e.g., label in the language of the importing country).requirements. To the best of our knowledge, Neogen products are compliant with applicable regulations in the countries where such products are sold.

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Dairy diagnostic products used in National Conference on Interstate Milk Shipments (NCIMS), a cooperative program involving FDA, state governments and the industry, must first be approved prior to commercialization. Before products requiring NCIMS approval can be sold in the U.S., extensive product performance data must be submitted in accordance with
FDA-approved
protocol administered by the AOAC Research Institute (AOAC RI). Following approval of a product by NCIMS, the product must be reviewed by the FDA. Our BetaStar Advanced U.S. dairy antibiotic residue testing product has been reviewed and/or approved by the appropriate regulatory bodies.

Many of the food safety diagnostic products do not require direct government approval. However, we have pursued AOAC approvalvoluntary approvals and certifications for a number of these products to enhance their marketability.

Neogen’s veterinary vaccine products and some pharmaceutical products require government approval to allow for lawful sales. The vaccine products are approved by the U.S. Department of Agriculture, Center for Veterinary Biologics

(USDA-CVB)
and theanalogous agencies in jurisdictions where sold. The pharmaceutical products are approved by the FDA.FDA and analogous agencies in jurisdictions where sold. The products, and the facilities in which they are manufactured, are in a position of good standing with bothall agencies. We have no warning letters based on any review of these products or facility inspection, no recalls on any of these products,inspections and are not aware of any reason why we could not manufacture and market such products in the future.

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Other animal safety and food safety products generally do not require additional registrations or approvals. However, Neogen’s regulatory staff routinely monitors amendments to current regulatory requirements to ensure compliance.

Human Capital Management

HUMAN CAPITAL MANAGEMENT

Our people are a critical component in our continued success. As a team, they put Neogen’s core values into action, while executing on key growth initiatives to maintain long-term sustainable growth. We strive to create a workplace of choice to attract, retain, and develop top talent to achieve our vision and deliver shareholder results. As of May 31, 2021,2023, we employed 1,841 full-time persons worldwide. None2,640 people worldwide, with 1,444 located in the U.S. and 1,196 international. We maintain good relations with both our union and non-union employees and have not experienced any work stoppages.

The Company is committed to fostering a diverse and inclusive workplace that attracts and retains exceptional talent. Through ongoing employee development, comprehensive compensation and benefits, and a focus on health, safety and employee wellbeing, the Company strives to help its employees in all aspects of these employees are covered by collective bargaining agreements.their lives so they can do their best work.

Workplace Culture and Employee Engagement. We adhere to a philosophy that includes, among other things, commitments to create ongoing job opportunities, pay fair wages, and protect worker health and safety. Fundamental to these commitments are Neogen’shave established our One Neogen Pillars of Trust consistingwhich are the principles that guide our decision-making every day: • Openness • Honesty • Credibility • Respect • Service. We value responsibility, consistency and integrity. Our Code of openness, honesty, credibility, respectConduct codifies our commitment to conducting business ethically.

Equity, Diversity, Inclusion, and service. Management considers its relations with employeesBelonging (EDIB). We strive to generallycreate an environment where colleagues feel valued and understand the important role we play in embracing diversity to improve the quality of our innovation, collaboration and relationships. We are dedicated to executing on our equity, diversity, inclusion and belonging initiatives.

Talent Attraction, Development and Retention. We employ a variety of career development, employee benefits, policies and compensation programs designed to attract, develop and retain our colleagues. Employee benefits and policies are designed for diverse needs. We have internal programs designed to develop and retain talent, including career planning, leadership development programs, performance management and training programs.

Compensation and Benefits. We strive to support our colleagues’ well-being and enable them to achieve their best at work and at home. Our compensation and benefits programs are designed to be positive.

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ITEM 1A.
RISK FACTORS
injuries to be investigated and for action plans to be implemented to mitigate potential recurrence. Our safety programs have resulted in strong safety performance.

ITEM 1A. RISK FACTORS

Investing in our securities involves a variety of risks and uncertainties, known and unknown, including, among others, those discussed below. Each of the following risks should be considered carefully, considered, together with all the other information included in this Annual Report on Form

10-K,
including our consolidated financial statements and the related notes and in our other filings with the SEC. Furthermore, additional risks and uncertainty not presently known to us or that we currently believe to be immaterial may also could adversely affect our business. Our business, results of operations, financial condition and cash flow could be materially and adversely affected by any of these risks or uncertainties.

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RISKS RELATING TO

COVID-19
The ongoing effects THE TRANSACTION WITH 3M CORPORATION

We may not realize the anticipated financial and other benefits, including growth opportunities, expected from the 3M Food Safety merger transaction.

On September 1, 2022, Neogen, 3M, and Neogen Food Safety Corporation, a wholly-owned subsidiary of 3M created to carve out 3M’s FSD, closed on the

COVID-19
pandemic could adversely affect our business, results Transaction combining 3M’s FSD with Neogen in a Reverse Morris Trust transaction and Neogen Food Safety Corporation became a wholly owned subsidiary of operations and financial condition.
Since March 2020,Neogen. Following the
COVID-19
pandemic has negatively impacted Transaction, pre-merger Neogen Food Safety Corporation stockholders owned, in the global economy, disrupted global supply chains, and created significant volatility and disruption of financial markets.
The extentaggregate, approximately 50.1% of the impactissued and outstanding shares of the
COVID-19
pandemic on our operationalNeogen common stock, and financial performance, including our ability to execute our business strategies and initiativespre-merger Neogen shareholders owned, in the expected time frame, continuesaggregate, approximately 49.9% of the issued and outstanding shares of Neogen common stock.

We have realized and expect that we will continue to dependrealize synergies, growth opportunities and other financial and operating benefits as a result of the Transaction. Our success in realizing these benefits, and the timing of their realization, depends, among other things, on manythe continued successful integration of the business operations of the 3M Food Safety business with Neogen. Even if we are able to integrate the 3M Food Safety business successfully, we cannot predict with certainty if or when the balance of these synergies, growth opportunities and other benefits will be realized, or the extent to which they will actually be achieved. For example, the benefits from the Transaction could be offset by costs incurred in integrating the 3M Food Safety business. Realization of any synergies, growth opportunities or other benefits could be affected by the factors outsidedescribed in other risk factors and a number of factors beyond our control, including, without limitation, the timing, extent, trajectorygeneral economic conditions, increased operating costs and durationregulatory developments.

The integration of the pandemic,3M Food Safety business with Neogen presents challenges, and the failure to successfully integrate the 3M Food Safety business could have a material adverse effect on our business, financial condition or results of operations.

Although significant progress has been made to date in the integration of the 3M Food Safety business with Neogen, there is much that remains to be accomplished, particularly in the integration of the manufacturing operations of the 3M Food Safety business with Neogen. There is a significant degree of difficulty inherent in the process of integrating the 3M Food Safety business with Neogen. The difficulties include:

the integration of the 3M Food Safety business with Neogen’s current businesses while carrying on the ongoing operations of all businesses;
managing a significantly larger company than before the consummation of the Transaction;
integrating the business cultures of the 3M Food Safety business and Neogen, which could prove to be incompatible;
creating uniform standards, controls, procedures, policies and information systems and controlling the costs associated with such matters;
the ability to ensure the effectiveness of internal control over financial reporting across the combined company;
integrating certain manufacturing, information technology, purchasing, accounting, finance, sales, billing, human resources, payroll and regulatory compliance systems; and
the potential difficulty in retaining key officers and personnel of Neogen and the 3M Food Safety business.

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The continued successful integration of the 3M Food Safety business cannot be assured. The failure to do so could have a material adverse effect on our business, financial condition or results of operations.

Pursuant to the terms of the Transaction, Neogen and formerly Neogen Food Safety Corporation will be restricted from taking certain actions that could adversely affect the intended tax treatment of the Transaction, and such restrictions could significantly impair Neogen’s and Neogen Food Safety Corporation’s ability to implement strategic initiatives that otherwise would be beneficial.

The Tax Matters Agreement executed in connection with the Transaction generally restricts Neogen and its affiliates from taking certain actions after the distribution of Neogen shares that could adversely affect the intended tax treatment of the Transaction. In particular:

For a two-year period following the distribution date, except as described below:

Neogen Food Safety Corporation will continue the active conduct of its trade or business and the trade or business of certain Neogen Food Safety Corporation subsidiaries;
Neogen Food Safety Corporation will not voluntarily dissolve or liquidate or permit certain Neogen Food Safety Corporation subsidiaries to voluntarily dissolve or liquidate;
Neogen and Neogen Food Safety Corporation will not enter into any transaction or series of transactions (or any agreement, understanding or arrangement) as a result of which one or more persons would acquire (directly or indirectly) stock comprising 50% or more of the vote or value of Neogen Food Safety Corporation or Neogen (taking into account the stock acquired pursuant to the merger);
Neogen and Neogen Food Safety Corporation will not engage in certain mergers or consolidations;
Neogen Food Safety Corporation will not, and will not permit certain Neogen Food Safety Corporation subsidiaries to, sell, transfer or otherwise dispose of 30% or more of the gross assets of Neogen Food Safety Corporation such subsidiaries, the Neogen Food Safety Corporation group or the active trade or business of Neogen Food Safety Corporation or certain Neogen Food Safety Corporation subsidiaries, subject to certain exceptions;
Neogen and Neogen Food Safety Corporation will not, and will not permit certain Neogen Food Safety Corporation subsidiaries to, redeem or repurchase stock or rights to acquire stock, unless certain requirements are met;
Neogen and Neogen Food Safety Corporation will not, and will not permit certain Neogen Food Safety Corporation subsidiaries to, amend their certificates of incorporation (or certain other organizational documents) or take any other action affecting the voting rights of any stock or stock rights of Neogen or Neogen Food Safety Corporation; and
Neogen and Neogen Food Safety Corporation will not, and will not permit any member of the Neogen Food Safety Corporation group or Neogen to, take any other action that would, when combined with any other direct or indirect changes in ownership of Neogen Food Safety Corporation and Neogen stock (including pursuant to the merger), have the effect of causing one or more persons to acquire stock representing 50% or more of the vote or value of Neogen Food Safety Corporation or Neogen, or otherwise jeopardize the tax-free status of the Transaction;
during the time period ending three years after the date of the distribution, Neogen Food Safety Corporation and Neogen also will be subject to certain restrictions relating to the SpinCo Business in Switzerland; and
Additionally, none of Neogen Food Safety Corporation, Neogen or any member of Neogen Food Safety Corporation group or Neogen may:
o
take, or permit to be taken, any action that could reasonably be expected to jeopardize the qualification of certain Neogen Food Safety Corporation debt as a security under Section 361(a) of the Code (other than making any payment permitted or required by the terms of the Neogen Food Safety Corporation debt);
o
permit any portion of certain nonqualified preferred stock to cease to be outstanding or modify the terms of such stock;

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unless, in each case, prior to taking any such action, Neogen and Neogen Food Safety Corporation shall have requested that 3M obtain, or request and receive 3M’s prior written consent to obtain, an IRS ruling satisfactory to 3M in its reasonable discretion or provide 3M with an unqualified tax opinion satisfactory to 3M in its sole and absolute discretion to the effect that such action would not jeopardize the intended tax treatment of the Transaction, unless 3M waives such requirement. Failure to adhere to these requirements could result in tax being imposed on 3M for which Neogen and Neogen Food Safety Corporation could bear responsibility and for which Neogen and Neogen Food Safety Corporation could be obligated to indemnify 3M. Any such indemnification obligation would likely be substantial and would likely have a material adverse effect on Neogen. These restrictions could have a material adverse effect on Neogen’s liquidity and financial condition, and otherwise could impair Neogen’s and Neogen Food Safety Corporation’s ability to implement strategic initiatives and Neogen Food Safety Corporation’s and Neogen’s indemnity obligation to 3M might discourage, delay or prevent a change of control that shareholders of Neogen may consider favorable.

RISKS RELATING TO OUR BUSINESS AND INDUSTRY

We are subject to risks relating to existing international operations and expansion into new geographical markets.

Expanding sales globally is part of our overall growth strategy, and we expect sales from outside the United States to continue to represent a significant portion of our revenue. In fiscal 2023, sales to customers outside of the U.S. accounted for 48.4% of our total revenue. Our international operations are subject to general risks related restrictions on travelto such operations, including:

political, social and transports, the developmenteconomic instability and availability of effective treatmentsdisruptions, including social unrest, geopolitical tensions, currency, inflation and vaccines, interest rate uncertainties;
government export controls, economic sanctions, embargoes or trade restrictions;
the imposition of protective public safety measures,duties and the impacttariffs and other trade barriers;
limitations on ownership and on repatriation or dividend of the pandemicearnings;
transportation delays and interruptions;
labor unrest and current and changing regulatory environments;
increased compliance costs, including costs associated with disclosure requirements and related due diligence;
difficulties in staffing and managing multi-national operations;
limitations on the global economy and consumer demand.
During the course of the pandemic, we modified our business practices to comply with safety measures required by federal, state, and local governments, as well as those we determine to be in the best interests of our employees and customers, including implementing social distancing, remote work, reducing employee travel, restricting building access, and more. In taking such precautionary actions, we may experience disruptions in our supply chain, operations, facilities, and workforce, which could negatively affect efficiency and productivity, cause delays in developing new products, our ability to marketenforce legal rights and remedies;
current products and services, and, ultimately, our stock price and financial performance.may not comply with product standards established by foreign regulatory bodies;
Additional future impactsdiffering labor regulations;
diminished protection of intellectual property in some countries;
access to us may include, butor control of networks and confidential information due to local government controls and vulnerability of local networks to cyber risks; and
fluctuations in foreign currency exchange rates.

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If we are not limitedunable to successfully manage the risks associated with expanding our global business or adequately manage operational risks of our existing international operations, these risks could have a material adverse effectseffect on the demand for our products and services,growth strategy into new geographical markets, our supply chain and sales and distribution channels, our cost structure and profitability. An extended period of global supply chain and economic disruption could materially affect our business, results of operations, and financial condition.

While we expect a solid recovery, in part due to increasing vaccination rates across the world, we also are aware that there may be a reduction in demand for our
COVID-19-related
products and services, including sanitizers, disinfectants, and wastewater testing as cases of
COVID-19
decrease.
The situation is changing rapidly, and future impacts may materialize that are not yet known. To the extent the
COVID-19
pandemic adversely affectsreputation, our business, results of operations, financial condition and stock price,cash flows. In addition, the impact of such risks could be outside of our control and could decrease our ability to sell products internationally, which could adversely affect our business, financial condition, results of operations or cash flows. For example, as a result of the ongoing military conflict between Russia and Ukraine and resulting heightened economic sanctions from the U.S. and the international community, we have discontinued sales into Russia and Belarus. The U.S. and other countries have imposed significant sanctions and could impose even wider sanctions and take other actions should the conflict further escalate. While it may also haveis difficult to anticipate the effect the sanctions announced to date could have on us, any further sanctions imposed or actions taken by the U.S. or other countries, including any expansion of heightening manysanctions beyond Russia and Belarus, could affect the global price and availability of the other risks described in this section.
RISKS RELATING TO OUR BUSINESS AND INDUSTRY
raw materials, reduce our sales and earnings or otherwise have an adverse effect on our business and results of operations.

Our business strategy is dependent on successfully promoting internal growth and identifying and integrating acquisitions.

Our business has grown significantly over the past several years as a result of both internal growth and acquisitions of existing businesses and their products. Management initiatives may be attempted to augment internal growth, such as strengthening our presence in select markets, reallocating research and development funds to products with higher growth potential, development of new applications for our technologies, enhancing our service offerings, continuing key customer efforts, and finding new markets for our products. Failure of these management initiatives may have a material adverse effect on our operating results and financial condition.

Identifying and pursuing acquisition opportunities, integrating these acquisitions into our business and managing their growth requires a significant amount of management’s time and skill. We cannot assure that we will be effective in identifying, integrating or managing future acquisition targets. Our failure to successfully integrate and manage a future acquisition maycould have a material adverse effect on our operating results and financial condition.

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In addition, if we continue to experience growth in our business, such growth could place a significant strain on our management, customer service, operations, sales and administrative personnel, and other resources. To serve the needs of our existing and future customers we will be required to recruit, train, motivate and manage qualified employees. We have incurred and will continue to incur significant costs to retain qualified management, sales and marketing, engineering, production, manufacturing and administrative personnel, as well as expenses for marketing and promotional activities. Our ability to manage our planned growth depends upon our success in expanding our operating, management, information and financial systems, which might significantly increase our operating expenses.

We may not be able to effectively manage our future growth, and if we fail to do so, our business, financial condition and results of operations could be adversely affected.

We rely significantly on our information systems’ infrastructure to support our operations and a failure of these systems and infrastructure and/or a security breach of our information systems could damage our reputation and have an adverse effect on operations and results.

We rely on our information systems’ infrastructure to integrate departments and functions, to enhance our ability to service customers, to improve our control environment, and to manage our cost reduction initiatives. If a security breach or cyberattack of our ITinformation technology ("IT") networks and systems occurs, our operations could be interrupted. Any issues involving our critical business applications and infrastructure maycould adversely impact our ability to manage our operations and the customers we serve. Although we have controls and security measures in place to prevent such attacks, experienced computer hackers are increasingly organized and sophisticated. Malicious attack efforts operate on a large-scalelarge scale and sometimes offer targeted attacks as a

paid-for
service. In addition, the techniques used to access or sabotage networks change frequently and generally are not recognized until launched against a target.

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We rely on several information systems throughout our company, as well as those of our third-party business partners, to provide access to our

web-based
products and services, keep financial records, analyze results of operations, process customer orders, manage inventory, process shipments to customers, store confidential or proprietary information and operate other critical functions. Although Neogen employswe employ system backup measures and engagesengage in information system redundancy planning and processes, such measures, as well as our current disaster recovery plan, may be ineffective or inadequate to address all vulnerabilities. Further, our information systems and our business partners’ and suppliers’ information systems may be vulnerable to attacks by hackers and other security breaches, including computer viruses and malware, through the Internetinternet (including via devices and applications connected to the Internet)internet), email attachments and persons with access to these information systems, such as our employees or third parties with whom we do business. As information systems and the use of software and related applications by us, our business partners, suppliers and customers become more cloud-based, there has been an increase in global cybersecurity vulnerabilities and threats, including more sophisticated and targeted cyber-related attacks that pose a risk to the security of our information systems and networks and the confidentiality, availability and integrity of data and information.

While we have implemented network security and internal control measures, especiallyincluding for the purpose of protecting our connected products and services from cyberattacks, and invested in our data and information technology infrastructure, there can be no assurance that these efforts will prevent a system disruption, attack, or security breach and, as such, the risk of system disruptions and security breaches from a cyberattack remains.

If our security and information systems are compromised, interrupted or destroyed, or employees fail to comply with the applicable laws and regulations, or thisthe information we maintain is obtained by unauthorized persons or used inappropriately, it could adversely affect our business and reputation, as well as our results of operations, and could result in litigation, the imposition of regulatory sanctions or penalties, or significant expenditures to remediate any damage to persons whose personal information has been compromised.

In addition,

fiscal year 2022, we began the implementation of our global SAP enterprise resource planning (ERP) system at our U.S. locations, which includes upgrades to many of our existing operating and financial systems. Such an implementation is a major undertaking, both financially and from a management and personnel perspective. Should the remaining systems not be implemented successfully, or if the systems do not perform in a satisfactory manner once implementation is complete, our business and operations could be disrupted and our results of operations could be adversely affected, including our ability to report accurate and timely financial results.

Pandemics or disease outbreaks, such as the COVID-19

may pandemic, have affected and could adversely affect our business, operation, results of operations and financial condition.

The COVID-19 pandemic negatively impacted the global economy, disrupted global supply chains, and created significant volatility and disruption of financial markets.

During the course of the pandemic, we modified our business practices to comply with safety measures required by federal, state and local governments, as well as those we determined to be in the best interests of our employees and customers, including implementing social distancing, remote work, reducing employee travel, restricting building access and more. In the event of the renewed outbreak of COVID-19 or an adverse impact on our information technology systems, including telecommuting issues associated with the rapid and broad-based shiftoutbreak of a different virus or disease, we could experience disruptions in our employee population working remotely,supply chain, operations, facilities and workforce which creates inherentcould cause delays in developing new products or negatively affect efficiency and productivity connectivityor our ability to market products and oversight challenges.

services, and, ultimately, our stock price and financial performance.

Additional future impacts to us may include, but are not limited to, material adverse effects on the demand for our products and services, our supply chain and sales and distribution channels, our cost structure and profitability. An extended period of global supply chain and economic disruption could materially affect our business, results of operations and financial condition.

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Disruption of our manufacturing and service operations could have an adverse effect on our financial condition and results of operations.

We manufacture our products at several manufacturing facilities located in the following locations: Lansing, Michigan; Lexington, Kentucky; Randolph, Wisconsin; Kenansville, North Carolina; Pleasantville, Iowa; Memphis, Tennessee; Turlock, California; Heywood, England; Liverpool, England; Ayr, Scotland; Rochdale, England; Bray, Ireland; and Pindamonhangaba, Brazil. We offer genomics services from facilities located in: Lincoln, Nebraska; Ayr, Scotland; Pindamonhangaba, Brazil; Edmonton, Canada; Shanghai, China; and Gatton, Australia. These

Our facilities and our distribution systems are subject to catastrophic loss due to fire, flood, terrorism or other natural or

man-made
disasters. If any of theseour facilities were to experience a catastrophic loss, it could disrupt our operations, delay production, shipments and revenue and result in significant expenses to repair or replace the facility and/or distribution system. If such a disruption were to occur, we could breach agreements, our reputation could be harmed, and our business and operating results could be adversely affected. Although we carry insurance for property damage and business interruption, we do not carry insurance or financial reserves for interruptions or potential losses arising from terrorism. Economic conditions and uncertainties in global markets maycould adversely affect the cost and other terms upon which we are able to obtain third party insurance. If we are unable to obtain sufficient and cost-effective third-party insurance coverage, or to the extent we have elected to self-insure, we maycould be at greater risk that our operations will be harmed by a catastrophic loss.
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Our dependence on suppliers could limit our ability to sell certain products or negatively affect our operating results.
We rely on third-party suppliers to provide raw materials and other components in our products, manufacture products that we do not manufacture ourselves and perform services that we do not provide ourselves. Because these suppliers are independent third parties with their own financial objectives, actions taken by them could have a negative effect on our results of operations. The risks of relying on suppliers include our inability to enter into contracts with third party suppliers on reasonable terms, inconsistent or inadequate quality control, relocation of supplier facilities, supplier work stoppages and suppliers’ failure to comply with their contractual obligations. In addition, we currently purchase some raw materials and products from sole or single sources. Some of the products that we purchase from these sources are proprietary and, therefore, cannot be readily or easily replaced by alternative sources. Problems with suppliers could negatively impact our ability to supply the market, substantially decrease sales, lead to higher costs or damage our reputation with our customers.

We rely heavily on third-party package delivery services, and a significant disruption in these services or significant increases in prices maycould disrupt our ability to ship products, increase our costs and lower our profitability.

We ship a significant portion of our products to customers through independent package delivery companies, such as UPS, Federal Express and DHL. We also ship our products through other carriers, including national and regional trucking firms, overnight carrier services and the U.S. Postal Service. If one or more of these third-party package delivery providers were to experience a major work stoppage, preventing our products from being delivered in a timely fashion or causing us to incur additional shipping costs we could not pass on to our customers, our costs could increase and our relationships with some of our customers could be adversely affected. In addition, if one or more of our third-party package delivery providers were to increase prices, and we were not able to find comparable alternatives or make adjustments within our delivery network, our profitability could be adversely affected.

Our dependence on suppliers could limit our ability to sell certain products or negatively affect our operating results.

We rely on third-party suppliers to provide raw materials and other components in our products, manufacture products that we do not manufacture ourselves and perform services that we do not provide ourselves. Because these suppliers are independent third parties with their own financial objectives, actions taken by them could have a negative effect on our results of operations. The risks of relying on suppliers include our inability to enter into contracts with third party suppliers on reasonable terms, inconsistent or inadequate quality control, relocation of supplier facilities, supplier work stoppages and suppliers’ failure to comply with their contractual obligations. In addition, we currently purchase some raw materials and products from sole or single sources. Some of the products that we purchase from these sources are proprietary and, therefore, cannot be readily or easily replaced by alternative sources. Problems with suppliers and the supply chain could negatively impact our ability to supply the market, substantially decrease sales, lead to higher costs or damage our reputation with our customers.

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Our business sells many products through distributors, which present risks that could negatively affect our operating results.

We sell many of our products, both within and outside of the U.S., through distribution.independent distributors. As a result, we are dependent on distributors to sell our products and assist us in promoting and creating a demand for our products. Our distributors sometimes offer products from several different companies, and those distributors may carry our competitors’ products and promote our competitors’ products over our own. We have limited ability, if any, to cause our distributors to devote adequate resources to promoting, marketing, selling and supporting our products. We cannot assure that we will be successful in maintaining and strengthening our relationships with our distributors or establishing relationships with new distributors who have the ability to market, sell, and support our products effectively. We may rely on one or more key distributors for a product or region, and the loss of one or more of these distributors could reduce our revenue. Distributors could face financial difficulties, including bankruptcy, which could impact our ability to collect our accounts receivable and negatively impact our financial results. In addition, violations of anti-bribery and anti-corruption or similar laws by our distributors could have a material impact on our business. Further, termination of a distributor relationship could result in increased competition in the applicable jurisdiction. Failing to manage the risks associated with our use of distributors could reduce sales, increase expenses and weaken our competitive position, which could have a negative impact on our operating results.

If we are unable to develop new products and technologies, our competitive position could be impaired, which could materially and adversely affect our sales and market share.

The markets in which we operate are characterized by changing technologies and the introduction of new products. As a result, our success is dependent upon our ability to develop or acquire new products and services on a cost-effective basis, to introduce them into the marketplace in a timely manner and to protect and maintain critical intellectual property assets related to these developments. Difficulties or delays in research, development or production of new products and technologies, or failure to gain market acceptance of new products and technologies, could significantly reduce future revenue and materially and adversely affect our competitive position. While we intend to continue to commit financial resources and effort to the development of new products entails substantial riskand services, we may not be able to successfully differentiate our products and services from those of failure dueour competitors. Our customers may not consider our proposed products and services to the productionbe of

non-viable
value to them or may not view them as superior to our competitors’ products lack of properly identifying market potential, and services. In addition, our competitors better serving the marketplace.
Our growth strategy includes significant investment inor customers could develop new technologies or products which address similar or improved solutions to our existing technologies. Further, we may not be able to adapt to evolving markets and expenditures for product development. To execute this strategy, we are continually developingtechnologies, develop new products, for which we believe there should be significant market demand. We cannot assure that we will successfully develop commercially viable products, that the products will be developed on a timely basis to meet market demandachieve and maintain technological advantages or that the relevant market will be properly identified. Our competitors may also adapt more quickly, and deliver superior technologies, price and/or service to better fit our customers’ requirements.protect technological advantages through intellectual property rights. If we expend substantial resources in developing an unsuccessful product, whether that lackdo not successfully compete through the development and introduction of success is the resultnew products and technologies, our business, results of operations, financial condition and cash flows could be materially adversely affected.

If we fail to maintain a positive reputation or are unable to conduct effective sales and marketing, our production of a

non-viable
product, a misidentified market, or a competitor’s superior ability to meet our customers’ requirements, operating resultsprospects and financial condition could be adversely affected.
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our brands have contributed significantly to the success of our business. We also believe that maintaining and enhancing these brands, especially market perceptions of the quality of our products, is critical to maintaining our competitive advantage. If any of our products are subject to recall or are proven to be, or are claimed to be, ineffective or inaccurate for their stated purpose, then this could have a material adverse effect on our business, financial condition or results of operations. Also, because we are dependent on market perceptions, negative publicity associated with product quality or other adverse effects resulting from, or perceived to be resulting from, our products could have a material adverse impact on our business, financial condition and results of operations.

Our sales and marketing efforts are anchored by promoting our products to potential customers. Therefore, our sales and marketing force, whether in-house sales representatives or third-party commercial partners, must possess an up-to-date understanding of industry trends and products, as well as promotion and communication skills. In addition, we have a network of third-party commercial partners that we use to sell or distribute our products.

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While we will continue to promote our brands to remain competitive, we may not be successful in doing so. If we are unable to increase or maintain the effectiveness and efficiency of our sales and marketing activities, or if we incur excessive sales expenses to do so, our business, financial condition and results of operations may be materially and adversely affected.

We could lose customers or generate lower revenue, operating profits and cash flows if there are significant increases in the cost of raw materials or if we are unable to obtain such raw materials or other components of our products.

We purchase raw materials and components for use in our products, which exposes us to volatility in prices for certain raw materials and products. Prices and availability of these raw materials are subject to substantial fluctuations that are beyond our control due to factors such as changing economic conditions, inflation, currency and commodity price fluctuations, tariffs, resource availability, transportation costs, weather conditions and natural disasters, political unrest and instability, and other factors impacting supply and demand pressures. Significant price increases for these supplies could adversely affect our operating profits. Current and future inflationary effects may be driven by, among other things, supply chain disruptions and governmental stimulus or fiscal policies. The COVID-19 pandemic, for example, resulted in raw material price inflation as well as supply chain constraints and disruptions. While we will generally attempt to mitigate the impact of increased raw materials prices by endeavoring to make strategic purchasing decisions, broadening our supplier base and passing along increased costs to customers, there may be a time delay between the increased raw material prices, the ability to increase the prices of products, and dependence on a sole or single source for certain materials and products. Additionally, we may be unable to increase the prices of products due to a competitor’s pricing pressure or other factors, or may be unable to raise the price of our products in a manner that is proportional to the level of inflation, which would materially adversely affect our results of operations.

Certain of our food safety product lines depend on a sole or single source suppliers and vendors. The ability of these third parties to deliver raw materials and products may also be affected by events beyond our control. In addition, public health threats, such as COVID-19, severe influenza and other highly communicable viruses or diseases could affect our supply of raw materials, by limiting our ability to transport raw materials from our vendors or increasing demand and competition for supplies, which could adversely affect our ability to obtain necessary raw materials for certain of our products. Any sustained interruption in our receipt of adequate raw materials, supply chain disruptions impacting the receipt or distribution of products, or disruption to key manufacturing sites’ operations due to natural and other disasters or events or other legal or regulatory requirements, could result in a significant price increase in raw materials, or their unavailability, which could result in a loss of customers or otherwise adversely impact our business, results of operations, financial condition and cash flows.

Our reputation, ability to do business and results of operations could be impaired by improper conduct by or disputes with any of our employees, agents or business partners and we have a compliance burden with respect to, and risk of violations of, anti-bribery, trade control, trade sanctions, anti-corruption and similar laws.

Our operations require us to comply with a number of U.S. and international laws and regulations, including those governing payments to government officials, bribery, fraud, anti-kickback and false claims, competition, export and import compliance, money laundering and data privacy, as well as the improper use of proprietary information or social media. In particular, our international operations are subject to the regulations imposed by the Foreign Corrupt Practices Act and the United Kingdom Bribery Act 2010 as well as anti-bribery and anti-corruption laws of various jurisdictions in which we operate. While we strive to maintain high standards, we cannot provide assurance that our internal controls and compliance systems always will protect us from acts committed by our employees, agents or business partners that would violate such U.S. or international laws or regulations or fail to protect our confidential information. Any such violations of law or improper actions could subject us to civil or criminal investigations in the U.S. or other jurisdictions, could lead to substantial civil or criminal, monetary and non-monetary penalties and related shareholder lawsuits, could lead to increased costs of compliance and could damage the our reputation, business, results of operations, financial condition and cash flows.

23


Tariffs and other trade measures could adversely affect our results of operations, financial position and cash flows.

Our international operations subject us to discriminatory or conflicting tariffs and trade policies. Tariffs have and may continue to increase our material input costs, and any further trade restrictions, retaliatory trade measures and additional tariffs could result in higher input costs to our products. We may not be able to fully mitigate the impact of these increased costs or pass price increases on to our customers. While tariffs and other trade measures imposed by other countries on U.S. goods have not yet had a significant impact on our business or results of operations, we cannot predict further developments, and such existing or future tariffs could have a material adverse effect on our results of operations, financial position and cash flows.

Changes in domestic and foreign governmental laws, regulations and policies, changes in statutory tax rates and laws, and unanticipated outcomes with respect to tax audits could adversely affect our business, profitability and reputation.

Our domestic and international sales and operations are subject to risks associated with changes in laws, regulations and policies (including environmental and employment regulations, export/import laws, tax policies and other similar programs). Failure to comply with any of the foregoing laws, regulations and policies could result in civil and criminal, monetary and non-monetary penalties, as well as damage to our reputation. In addition, we cannot provide assurance that our costs of complying with new and evolving regulatory reporting requirements and current or future laws, including environmental protection, employment, data security, data privacy and health and safety laws, will not exceed our estimates. While these risks or the impact of these risks are difficult to predict, any one or more of them could adversely affect our business, results of operations and reputation.

We are subject to taxation in a number of jurisdictions. Accordingly, our effective tax rate is impacted by changes in the mix among earnings in countries with differing statutory tax rates. A material change in the statutory tax rate or interpretation of local law in a jurisdiction in which we have significant operations could adversely impact our effective tax rate and impact our financial results.

Our tax returns are subject to audit and taxing authorities could challenge our operating structure, taxable presence, application of treaty benefits or transfer pricing policies. If changes in statutory tax rates or laws or audits result in assessments different from amounts estimated, our business, results of operations, financial condition and cash flows could be adversely affected. In addition, changes in tax laws could have an adverse effect on our customers, resulting in lower demand for our products and services.

A deterioration in our future expected profitability or cash flows could result in an impairment of our recorded goodwill and intangible assets.

We have significant goodwill and intangible assets recorded on our consolidated balance sheet. The valuation and classification of these assets and the assignment of useful lives to intangible assets involve significant judgments and the use of estimates. Impairment testing of goodwill and intangible assets requires significant use of judgment and assumptions, particularly as it relates to the determination of fair market value. A decrease in the long-term economic outlook and future cash flows of our business could significantly impact asset values and potentially result in the impairment of intangible assets, including goodwill.

The markets for our products are extremely competitive, and our competitors could use existing resource advantages to our detriment.

The markets in which we competefood and animal safety industries are subject to rapid and substantial changes in technology and are characterized by extensive research and development and intense competition. Our competitors and potential competitors may have greater financial, technical, manufacturing, marketing, research and development and management resources than we do.us. These competitors could use their resources, reputations and ability to leverage existing customer relationships to give themprovide a competitive advantage over us.us that could impact our results of operations. They might also succeed in developing products that are more reliable and effective than our products, are less costly than our products or provide alternatives to our products.

If the products of a competitor are better able to meet our customers' requirements, then our operating results could be adversely affected.

24


We are dependent on the agricultural marketplace, which is affected by factors beyond our control.

Our primary customers are in the agricultural and food production industries. Economic conditions affecting agricultural industries are cyclical and are dependent upon many factors outside of our control, including weather conditions, changes in consumption patterns or commodity prices. Any of these factors in the agricultural marketplace could affect our sales and overall financial performance.

RISKS RELATED TO AN INVESTMENT IN OUR SECURITIES

LIQUIDITY, INDEBTEDNESS AND THE CAPITAL MARKETS

We have incurred substantial indebtedness and our financial condition and operations may be adversely affected by a violation of financial and other covenants.

We have incurred substantial indebtedness and related debt service obligations, which could have important consequences, including:

reduced flexibility in responding to changing business and economic conditions, and increased vulnerability to general adverse economic and industry conditions;
reduced flexibility in planning for, or reacting to, changes in our business, the competitive environment and the markets in which we operate, and to technological and other changes;
reduced access to capital and increasing borrowing costs generally or for any additional indebtedness to finance future operating and capital expenditures and for general corporate purposes;
lowered credit ratings;
reduced funds available for operations, capital expenditures and other activities;
increased vulnerability to increases in interest rates in general because a substantial portion of our indebtedness is expected to bear interest at floating rates; and
competitive disadvantages relative to other companies with lower debt levels.

Our Term Loan, comprised of our Revolving Facility and Term Loan Facility, contain customary affirmative and negative covenants. Some or, with respect to certain covenants, all of these agreements include financial covenants based on leverage and cash interest expense coverage ratios and limitations to make certain investments, declare or pay dividends or distributions on capital stock, redeem or repurchase capital stock and certain debt obligations, incur liens, incur indebtedness, or merge, make certain acquisitions or sales of assets.

The Senior Notes governing our senior unsecured indebtedness also include customary events of default. A violation of any of these covenants or agreements could result in a default under these contracts, which could permit the lenders or note holders, as applicable, to accelerate repayment of any borrowings or notes outstanding at that time and levy on the collateral granted in connection with the Senior Notes. A default or acceleration under the Senior Notes governing the senior unsecured indebtedness could result in defaults under our other debt agreements and could adversely affect our ability to operate our business, our subsidiaries' ability to operate their respective businesses and our results of operations and financial condition.

The available capacity under our Revolving Facility could be limited by our covenant ratios under certain conditions. An increase in the applicable leverage ratio, as a result of decreased earnings or otherwise, could result in reduced access to capital under our Revolving Facility, which is a significant component of our total available liquidity.

25


Our quarterly or annual operating results are subject to significant fluctuations.

We have experienced, and may experience in the future, significant fluctuations in our quarterly or annual operating results. The mix of products sold and the acceptance of new products, in addition to other factors such as cost increases, could contribute to this variability. We operate with relatively little backlog and have few long-term customer contracts.contracts and operate primarily with purchase orders. Substantially all our product revenue in each period results from orders received in that period. In addition, our expense levels are based, in part, on our expectation of future revenue levels. Therefore, a shortfall in expected revenue could result in a disproportionate decrease in our net income.

The market price of our common stock maycould be highly volatile.

The trading price of our common stock maycould be volatile. Securities markets worldwide experience significant price and volume fluctuations. This market volatility, as well as other general economic, market or political conditions, could reduce the market price of our common stock rapidly and unexpectedly, despite our operating performance. Factors that maycould impact the market price of our common stock include the factors described in this “Risk Factors” section and elsewhere in this Annual Report on Form

10-K,
as well as:

Public announcements (including the timing of these announcements) regarding our business, financial performance, acquisitions and prospects or new products or services, product enhancements or technological advances by our competitors or us;
Trading activity in our stock, including transactions by us, our executive officers and directors, and significant stockholders;shareholders; trading activity that results from the ordinary course rebalancing of stock indices in which we may be included, such as the S&P
Mid-Cap
400 Index; trading activity related to our inclusion in, or removal from, any stock indices; and short-interest in our common stock, which could be significant from time to time;
��
Investor perception of us and the industry and markets in which we operate, including changes in earnings estimates or buy/sell recommendations by securities analysts; and whether or not we meet earnings estimates of securities analysts who follow us; and
General financial, domestic, international, economic and market conditions, including overall fluctuations in the U.S. equity markets, which may experience extreme volatility that, in some cases, is unrelated or disproportionate to the operating performance of particular companies.

Our business could be adversely affected by fluctuations in the global capital markets.

Our business and financial results are affected by fluctuations in the global financial markets, including interest rates and currency exchange rates. The exposure to fluctuations in currency exchange rates takes on different forms. International revenues and costs are subject to the risk that fluctuations in exchange rates could adversely affect our reported revenues and profitability when translated into U.S. dollars for financial reporting purposes. These fluctuations could also adversely affect the demand for products and services provided by us. Failure to respond timely to these fluctuations, or failure to effectively hedge these risks when possible, could lead to a material adverse impact on our results of operations and financial condition.

We cannot assure investors that we will make dividend payments in the future.

Dividend payments to our shareholders depend upon a number of factors, including our results of operations, cash flows and financial position, contractual restrictions and other factors considered relevant by our Board of Directors. We have not historically paid dividends to our shareholders, and there is no assurance that we will declare and pay, or have the ability to declare and pay, any dividends on our common stock in the future.

26


Certain shareholders could attempt to influence changes within Neogen, which could adversely affect our operations, financial condition and the value of our common stock.

Our shareholders may from time-to-time seek to acquire a controlling stake in Neogen, engage in proxy solicitations, advance shareholder proposals or otherwise attempt to effect changes. Campaigns by shareholders to effect changes at publicly-traded companies are sometimes led by investors seeking to increase short-term shareholder value through actions such as financial restructuring, increased debt, special dividends, stock repurchases or sales of assets or the entire company. Responding to proxy contests and other actions by activist shareholders can be costly and time-consuming, and could disrupt our operations and divert the attention of our Board of Directors and senior management from the pursuit of our business strategies. These actions could adversely affect our operations, financial condition and the value of our common stock.

GENERAL RISKS

RISK FACTORS

We have identified a material weakness in our internal control over financial reporting, and if we are unable to improve our internal controls, our financial results may not be accurately reported.

As disclosed in Item 9A, “Controls and Procedures,” we identified material weaknesses in our internal control over financial reporting related to ineffective information technology general controls, our period-end invoice accrual procedures, and ineffective operation of management review controls related to the accounting, valuation and purchase price allocation of the Company’s acquisition and associated goodwill. The material weaknesses did not result in any material identified misstatements to the consolidated financial statements, and there were no changes to previously issued financial results. We are actively developing a remediation plan designed to address these material weaknesses, however, we cannot guarantee that these steps will be sufficient or that we will not have material weaknesses in the future. These material weaknesses, or difficulties encountered in implementing new or improved controls or remediation, could prevent us from accurately reporting our financial results, result in material misstatements in our financial statements or cause us to fail to meet our reporting obligations. Failure to comply with Section 404 of the Sarbanes-Oxley Act of 2002 could negatively affect our business, financial condition and results of operations.

Our success is highly dependent on our ability to obtain protection for the intellectual property utilizedused in our products; these products could be the subject of patent infringement challenges.

Our success and ability to compete depends, in part, on our ability to obtain protectionprotect, in the U.S. and other countries, for our products by establishing and maintaining intellectual property rights capable of protecting our technology and products. Patent applications filed by us may not result in the issuance of patents or, if granted, may not be granted in a form that will be commercially advantageous to us. Even if granted, patents can be challenged, narrowed, invalidated, or circumvented, which could limit our ability to stop competitors from marketing similar products or limit the length of time we have patent protection for our products. We also cannot assure that our nondisclosure agreements, together with trade secrets and other common law rights, will provide meaningful protection for our trade secrets and other proprietary information. Moreover, the laws of some foreign jurisdictions may not protect intellectual property rights to the same extent as in the U.S., and many companies have encountered significant difficulties in protecting and defending such rights in foreign jurisdictions. If we encounter such difficulties or we are otherwise precluded from effectively protecting our intellectual property rights domestically or in foreign jurisdictions, we could incur substantial costs and our business, including our business prospects, could be substantially harmed.

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From time to time, we have received notices alleging that our products infringe third-party proprietary rights. Whether the manufacture, sale, or use of current products, or whether any products under development would, upon commercialization, infringe any patent claim cannot be known with certainty unless and until a court interprets thea patent claim and its validity in the context of litigation. When an infringement allegation is made against us, we may seek to invalidate the asserted patent claim and/or to allege

non-infringement
of the asserted patent claim. For us to invalidate a U.S. patent claim, we would need to rebut the presumption of validity afforded to issued patents in the U.S. with clear and convincing evidence of invalidity, which is a high burden of proof. The outcome of infringement litigation is subject to substantial uncertainties, and also the testimony of experts as to technical facts upon which experts may reasonably disagree. Our defense of an infringement litigation lawsuit could result in significant expense. Regardless of the outcome, infringement litigation could significantly disrupt our marketing, development and commercialization efforts, divert management’s attention and consume our financial resources. In the event that we are found to infringe any valid claim in a patent held by a third party, we could, among other things, be required to:

Pay damages, including up to treble damages and the other party’s attorneys’ fees, which may be substantial;

27


Cease the development, manufacture, importation, use and sale of products that infringe the patent rights of others, through a court-imposed injunction;
Expend significant resources to redesign our technology so that it does not infringe others’ patent rights, or develop or acquire
non-infringing
intellectual property, which may not be possible;
Discontinue manufacturing or other processes incorporating infringing technology; and/or
Obtain licenses to the infringed intellectual property, which may not be available to us on acceptable terms, or at all.

Any development or acquisition of

non-infringing
products, technology or licenses could require the expenditure of substantial time and other resources and could have a material adverse effect on our business and financial results. If we are required to, but cannot, obtain a license to valid patent rights held by a third party, we would likely be prevented from commercializing the relevant product, or from further manufacture, sale or use of the relevant product.

We are subject to substantial governmental regulation.

A portion of our products and facilities are regulated by various domestic and foreign government agencies including but not limited to, the U.S. Department of Agriculture, the U.S. Food and Drug Administration and the Environmental Protection Agency. A significant portion of our revenue is derived from products used to monitor and detect the presence of residuessubstances that are regulated by various government agencies. Furthermore, our growth maycould result in substantial liability to us and be adversely affected by the implementation of new regulations. The costs of compliance or failure to comply with any obligations related to these laws or regulations could adversely impact our business.

We are dependentbusiness, including suspension or cessation of our operations, restrictions on our ability to expand at our present locations or require us to make significant capital expenditures or incur other significant expenses.

Failure to attract, retain and develop personnel, including for key employees.

management positions, could have an adverse impact on our results of operations, financial condition and cash flows.

Our success depends,growth, profitability and effectiveness in largeconducting our operations and executing our strategic plans depend in part on members of our ability to attract, retain and develop qualified personnel and align them with appropriate opportunities for key management team.positions and support for strategic initiatives. Our loss of any of these, or otherour key employees could have a material adverse effect on us. We have not executed long-term employment agreements with any of these employees and do not expect to do so in the foreseeable future. Our success depends, significantly, onWe compete with employers in various industries for sales, manufacturing, technical services or other personnel, and this competition to hire may increase and the availability of qualified personnel may be reduced. If we are unsuccessful in our ability to continueefforts to attract and retain such personnel.qualified personnel, our business, results of operations, financial condition, cash flows and competitive position could be adversely affected. Additionally, we could miss opportunities for growth and efficiencies. We cannot assure that we will be able to retain our existing personnel or attract additional qualified persons when required and on acceptable terms.

Our business may be subject to product or servicesservice liability claims.

The manufacturing and distribution of our products or performance of our services involves an inherent risk of liability claims being asserted against us. Regardless of whether we are ultimately determined to be liable or our products are determined to be defective, we mightcould incur significant legal expenses not covered by insurance. In addition, product or service liability litigation could damage our reputation and impair our ability to market our products and services, regardless of the outcome. Litigation also could also impair our ability to retain product liability insurance or make our insurance more expensive. Although we currently maintain liability insurance, we cannot assure that we will be able to continue to obtain such insurance on acceptable terms, or that such insurance will provide adequate coverage against all potential claims. If we are subject to an uninsured or inadequately insured product or services liability claim, our business, financial condition and results of operations could be adversely affected.

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Our international operations are subject to different product standards as well as other operational risks.
In fiscal 2021, sales to customers outside of the U.S. accounted for 39.1% of our total revenue. We expect that our international business will continue to account for a significant portion of our total sales. Foreign regulatory bodies may establish product standards different from those in the U.S. and with which our current products do not comply. Our potential inability to design products that comply with foreign standards could have a material adverse effect on our future growth. Other risks related to sales to customers outside of the U.S. include possible disruptions in transportation, difficulties in building and managing foreign distribution, fluctuation in the value of foreign currencies, changes in import duties and quotas and unexpected economic and political changes in foreign markets. These factors could negatively impact our competitiveness in these markets or otherwise adversely impact our business results or financial condition. Moreover, discriminatory or conflicting fiscal or trade policies in different countries, including potential changes to tariffs and existing trade policies and agreements, could adversely affect our results.

Changing political conditions could adversely impact our business and financial results.

Changes in the political conditions in markets in which we manufacture, sell or distribute our products maycould be difficult to predict and may adverselycould affect our business and financial results. For example, the U.K.’s decision to leave the European Union has created uncertainty regarding, among other things, the U.K.’s future legal and economic framework and how the U.K. will interact with other countries, including with respect to the free movement of goods, services, capital and people.results adversely. In addition, results of elections, referendums or other political processes in certain markets in which our products are manufactured, sold, or

28


distributed could create uncertainty regarding how existing governmental policies, laws and regulations may change, including with respect to sanctions, taxes, the movement of goods, services, capital and people between countries and other matters. The potential implications of such uncertainty, which include, among others, exchange rate fluctuations, trade barriers and market contraction, could adversely affect the Company’sour business and financial results.

Climate change, or legal, regulatory or market measures to address climate change maycould materially adversely affect our financial condition and business operations.

Climate change resulting from increased concentrations of carbon dioxide and other greenhouse gases in the atmosphere could present risks to our future operations from natural disasters and extreme weather conditions, such as hurricanes, tropical storms, blizzards, tornadoes, earthquakes, wildfires or flooding. Such extreme weather conditions could pose physical risks to our facilities and disrupt operation of our supply chainoperations and impair our critical systems, and may impact raw material sourcing, manufacturing operations, the distribution of our products and our operational costs. Damage or destruction of our facilities may result in losses that exceed our insurance coverage. The impacts of climate change on global water resources may result in water scarcity, which could in the future impact our ability to access sufficient quantities of water in certain locations and result in increased costs. Concern over climate change could result in new legal or regulatory requirements designed to mitigate the effects of climate change on the environment. If such laws or regulations are more stringent than current legal or regulatory requirements, we may experience increased compliance burdens and costs to meet the regulatory obligations and mayobligations.

Our business could be adversely affect raw material sourcing, manufacturing operations andimpacted by an inability to meet the distributionexpectations of our products.

stakeholders related to environmental, social and governance (ESG) objectives.

Various stakeholders, including customers, suppliers, providers of debt and equity capital, regulators, and those in the workforce, are increasing their expectations of companies to do their part to combat global climate change and its impact and to conduct their operations in an environmentally sustainable and socially responsible manner with appropriate oversight by senior leadership. We have made certain public commitments to reduce emissions, conserve resources at our various facilities and further develop a diverse, equitable and inclusive culture. A failure to respond to the expectations and initiatives of our stakeholders or to achieve the commitments we have made, could result in damage to our reputation and relationships with various stakeholders, as well as adversely impact our financial condition due to volatility in the cost or availability of capital, difficultly obtaining new business, or entering into new supplier relationships, a possible loss of market share on our current product portfolio, or difficulty attracting and retaining a skilled workforce.

Tax legislation could materially adversely affect our financial results and tax liabilities.

We are

Our business is subject to thetax-related external conditions, such as tax rates, tax laws, and regulations, changing political environments in the U.S. and foreign jurisdictions that impact tax examination, assessment and enforcement approaches. In addition, changes in tax laws including further regulatory developments arising from U.S. tax reform legislation and/or regulations around the world could result in a tax expense or benefit recorded to our consolidated statement of earnings. In connection with guidance such as the Base Erosion and Profit Shifting (BEPS) Integrated Framework provided by Organization for Economic Cooperation and Development (OECD), determination of multi-jurisdictional taxation rights and the rate of tax applicable to certain types of income may be subject to potential change. Due to uncertainty of the U.S., including stateregulation changes and local governments, as well as foreign jurisdictions. Legislation may be enacted that could materially adversely affectother tax-related factors stated above, it is currently not possible to assess the ultimate impact of these actions on our financial results There can be no assurance that our effective tax rate will not be adversely affected by legislation.

Our tax expense and liabilities may also be affected by other factors, such as changes in our business operations, acquisitions, investments, entry into new businesses and geographies, intercompany transactions, the relative amount of our foreign earnings, losses incurred in jurisdictions for which we are not able to realize related tax benefits, changes in our stock price, and changes in our deferred tax assets and liabilities and their valuation. In addition, tax laws and regulations are extremely complex and subject to varying interpretations. For example, the legislation known as the U.S. Tax Cuts and Jobs Act of 2017 (the “U.S. Tax Act”) requires complex computations to be performed that were not previously required by U.S. tax law, significant judgments to be made in interpretation of the provision of the U.S. Tax Act, significant estimates in calculations, and the preparation and analysis of information not previously relevant or regularly produced. The U.S. Treasury Department, the IRS, and other standard-setting bodies will continue to interpret or issue guidance on how provisions of the U.S. Tax Act will be applied or otherwise administered. As future guidance is issued, we may make adjustments to amounts that we have previously recorded that may materially impact our financial statements in the period in which the adjustments are made.
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Table of Contents
statements.

Although we believe that our historical tax positions are sound and consistent with applicable laws, regulations and existing precedent, there can be no assurance that our tax positions will not be challenged by relevant tax authorities or that we would be successful in any such challenge. Additionally, we operate in multiple income tax jurisdictions and must determine the appropriate allocation of income to each of these jurisdictions based on current interpretations of complex income tax regulations. Income tax audits associated with the allocation of income and other complex issues maycould result in significant income tax adjustments that could negatively impact our future operating results.

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Table of Contents
ITEM 1B.
UNRESOLVED STAFF COMMENTS – NONE
ITEM 2.
PROPERTIES

ITEM 1B.UNRESOLVED STAFF COMMENTS – NONE

ITEM 2.PROPERTIES

Principal Manufacturing, Distribution and Administrative locations

Location
Square
Feet
Operations
Ownership
Lansing, Michigan
300,000Corporate, Food Safety, Animal SafetyOwned
Lexington, Kentucky
210,000Animal SafetyOwned
Kenansville, North Carolina
33,500Animal SafetyLeased, expires 3/2022
St Joseph, Michigan
7,000Animal SafetyLeased, expires 12/2023
Randolph, Wisconsin
137,000Animal SafetyOwned
Pleasantville, Iowa
59,000Animal SafetyLeased, expires 12/2022
Lincoln, Nebraska
41,000Animal SafetyOwned
Memphis, Tennessee
66,100Animal SafetyOwned
Turlock, California
29,500Animal SafetyLeased, expires 9/2022
Edmonton, Alberta, Canada
4,800Animal SafetyOwned
Ayr, Scotland, United Kingdom
74,000Food SafetyOwned
Heywood, England, United Kingdom
26,800Food SafetyOwned
Rochdale, England, United Kingdom
60,000Food SafetyOwned
Liverpool, England, United Kingdom
4,000Food SafetyLeased, expires 12/2025
Milan, Italy
1,000Food SafetyLeased, expires 01/2022
Bray, Ireland
39,000Food SafetyOwned
Indaiatuba, Brazil
6,800Food SafetyLeased, month to month
Pindamonhangaba, Brazil
76,000Food SafetyOwned
Naucalpan, Mexico
27,000Food SafetyLeased, expires 10/2021
Buenos Aires, Argentina
7,500Food SafetyLeased, expires 8/2023
Ciudad de la Costa, Uruguay
3,200Food SafetyLeased, expires 09/2022
Santiago, Chile
3,200Food SafetyLeased, expires 3/2022
Shanghai, China
7,900Food SafetyLeased, expires 10/2021
Kochi, India
5,500Food SafetyLeased, month to month
Kochi, India
4,000Food SafetyOwned
Gatton, Australia
4,600Animal SafetyLeased, expires 1/2023
Ipswitch, Australia
30,000Animal SafetyOwned
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Table of Contents
locations:

Location

 

Owned

 

 

Leased

 

 

Segment

U.S.

 

 

7

 

 

 

7

 

 

Corporate, Food Safety, Animal Safety

Canada

 

 

1

 

 

 

0

 

 

Animal Safety

U.K.

 

 

4

 

 

 

3

 

 

Food Safety

Ireland

 

 

1

 

 

 

0

 

 

Food Safety

Italy

 

 

0

 

 

 

1

 

 

Food Safety

UAE

 

 

0

 

 

 

1

 

 

Food Safety

Brazil

 

 

2

 

 

 

0

 

 

Food Safety

Mexico

 

 

0

 

 

 

2

 

 

Food Safety

Guatemala

 

 

0

 

 

 

1

 

 

Food Safety

Argentina

 

 

0

 

 

 

1

 

 

Food Safety

Uruguay

 

 

0

 

 

 

1

 

 

Food Safety

Chile

 

 

0

 

 

 

1

 

 

Food Safety

Colombia

 

 

0

 

 

 

1

 

 

Food Safety

China

 

 

0

 

 

 

1

 

 

Food Safety

India

 

 

1

 

 

 

1

 

 

Food Safety

Korea

 

 

0

 

 

 

1

 

 

Food Safety

Thailand

 

 

0

 

 

 

1

 

 

Food Safety

Australia

 

 

2

 

 

 

0

 

 

Animal Safety

Total

 

 

18

 

 

 

23

 

 

 

Our corporate headquarters are located in Lansing, Michigan, with administrative, sales, manufacturing, and warehousing in other locations domestically and globally. These properties are in good condition, well-maintained, and generally suitable and adequate to support our business. For thoseleased properties, we do not anticipate difficulty in renewing existing leases expiring within the next 12 months, we believe that we will be able to negotiate agreements to extend such leases on similar terms.

ITEM 3.
LEGAL PROCEEDINGS
Neogenor in finding alternative facilities.

ITEM 3.LEGAL PROCEEDINGS

The litigation process is subject to certain legal proceedings inmany uncertainties, and the normal courseoutcome of business that, in the opinion of management, shouldindividual matters is not have a material effect on our future results of operations or financial position. On March 6, 2020, the Company received an administrative subpoena from the U.S. Treasury Department’s Office of Foreign Assets Control (OFAC) regarding activities or transactions involving parties located in Iran. The Company subsequently conducted an internal investigation under the direction of outside legal counselpredictable with assurance. See Note 7. “Commitments and disclosed information concerning certain genomic testing services provided to an unrelated U.S.-based party engaged in veterinary activities involving an Iranian party. The Company continues to cooperate with OFAC’s investigation and is currently examining whether certain of these activities may be eligible for OFAC General Licenses authorizing agricultural and veterinary activities. In addition to respondingContingencies” to the administrative subpoena, the Company is implementing additional compliance measures to prevent inadvertent dealings with restricted countries or parties. These measures will further enhance the Company’s international trade compliance program, which is designed to assure that the Company does not conduct business directly or indirectly with any countries or parties subject to U.S. economic sanctionsconsolidated financial statements included in Item 15. “Exhibits and export control laws. Although it is too early to predict what action, if any, that OFAC will take, the Company does not currently have any reason to believe that OFAC’s pending investigation will have a meaningful impact on its operations, the resultsFinancial Statement Schedules” of operationsthis Report for any future period, or its overall financial condition. In fiscal 2020, the Company took a charge to expense and recorded a reservediscussion of $600,000 to provide for potential fines or penalties on this matter. At this time, the Company believes that it is adequately reserved for this issue.

ITEM 4.
MINE SAFETY DISCLOSURES — NOT APPLICABLE
loss contingencies.

ITEM 4.MINE SAFETY DISCLOSURES — NOT APPLICABLE

30


PART II

ITEM 5.
MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

ITEM 5. MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

Market Information

Neogen Common Stock is traded on the NASDAQ Global Select Market under the symbol NEOG.

Holders

As of June 30, 2021,2023, there were approximately 221580 stockholders of record of Common Stockour common stock. The actual number of holders is significantly greater than this number of holders and management believes thereincludes stockholders who are a total of approximately 10,000 beneficial holders.

owners but whose shares are held in street name by brokers and other nominees.

Dividends

Neogen has never paid cash dividends on its Common Stock.

22

Table of Contents
Stock and does not expect to pay dividends in the foreseeable future.

Securities Authorized for Issuance under Equity Compensation Plans

The graph below matches Neogen Corporation’s cumulative

5-Year
total shareholder return on common stock with the cumulative total returns of the NASDAQ Composite index and the NASDAQ Medical Equipment index. The graph tracks the performance of a $100 investment ininformation regarding our common stock and in each index (with the reinvestment of all dividends) from 5/31/2016 to 5/31/2021.
   
5/16
   
5/17
   
5/18
   
5/19
   
5/20
   
5/21
 
Neogen Corporation
  
 
100.00
 
  
 
128.20
 
  
 
204.47
 
  
 
152.18
 
  
 
192.34
 
  
 
249.30
 
NASDAQ Composite
  
 
100.00
 
  
 
126.75
 
  
 
153.80
 
  
 
155.70
 
  
 
200.33
 
  
 
292.39
 
NASDAQ Medical Equipment
  
 
100.00
 
  
 
133.48
 
  
 
188.69
 
  
 
184.23
 
  
 
224.92
 
  
 
312.79
 
The stock price performance included in this graphsecurities authorized for issuance under equity compensation plans is not necessarily indicative of future stock price performance.
23

Table of Contents
ITEM 6.
SELECTED FINANCIAL DATA
The following tables set forth selected consolidated financial data of Neogen for the year ended May 31, 2021, and each of the four preceding fiscal years. The selected consolidated financial data presented below have been derivedincorporated by reference from our consolidated financial statements. This financial data should be read in conjunction with the consolidated financial statements, related notes and other financial information appearing elsewhere in this Form
10-K.
   
Year Ended May 31
 
   
2021
   
2020
   
2019
   
2018
  
2017
 
(in thousands, except per share data)
                   
Income Statement Data:
         
Food Safety Revenues
  $234,244   $212,691   $213,474   $194,477  $170,034 
Animal Safety Revenues
   234,215    205,479    200,712    203,453   188,243 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Total Revenues
   468,459    418,170    414,186    397,930   358,277 
Total Cost of Revenues
   253,403    221,891    222,266    211,658   189,353 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Gross Margin
   215,056    196,279    191,920    186,272   168,924 
Sales and Marketing
   73,443    69,675    70,230    66,929   59,380 
General and Administrative
   51,197    44,331    40,791    38,294   34,214 
Research and Development
   16,247    14,750    12,805    10,855   10,385 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Operating Income
   74,169    67,523    68,094    70,194   64,945 
Other Income
   1,099    4,782    4,865    3,271   1,728 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Income Before Income Taxes
   75,268    72,305    72,959    73,465   66,673 
Provision for Income Taxes
   14,386    12,830    12,783    10,250   22,700 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Net Income
   60,882    59,475    60,176    63,215   43,973 
Net (Income) Loss Attributable to
Non-controlling
Interest
   —      —      —      (70  (180
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Net Income Attributable to Neogen
  $60,882   $59,475   $60,176   $63,145  $43,793 
  
 
 
   
 
 
   
 
 
   
 
 
  
 
 
 
Net Income per Share (basic) (1)
  $0.57   $0.57   $0.58   $0.62  $0.43 
Net Income per Share (diluted) (1)
  $0.57   $0.56   $0.57   $0.61  $0.43 
Weighted Average Shares Outstanding (diluted) (1)
   107,120    105,720    104,850    104,298   102,330 
   
Year Ended May 31
 
   
2021
   
2020
   
2019
   
2018
  
2017
 
Balance Sheet Data:
         
Cash and Cash Equivalents and Marketable Securities
  $381,087   $343,673   $267,524   $210,810  $143,635 
Working Capital (2)
   537,852    488,917    411,278    337,101   256,959 
Total Assets
   920,192    797,182    695,740    618,009   528,409 
Long-Term Debt
   —      —      —      —     —   
Total Equity
   840,377    725,177    637,899    560,175   471,757 
(1)
On December 29, 2017, the Company effected a
4-for-3
stock split whereby shareholders of record on December 18, 2017 received a dividend of one additional share of stock for each three shares held. On June 4, 2021, the Company effected a
2-for-1
stock split whereby shareholders on record as of May 26, 2021 received a dividend of one additional share of common stock for each share held. All share and per share amounts in this Form
10-K
have been adjusted to reflect both stock splits as if they had taken place at the beginning of the periods presented.
(2)
Defined as current assets less current liabilities.
24
Proxy Statement.

ITEM 6. RESERVED

31


Table of Contents
ITEM 7.
MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

The following discussion and analysis of our financial condition and results of operations should be read in conjunction with the consolidated financial statements and related notes appearing elsewhere in this Annual Report on Form

10-K.

In addition, any forward-looking statements represent management’s views only as of the day this Form

10-K
was first filed with the Securities and Exchange Commission and should not be relied upon as representing management’s views as of any subsequent date. While we may elect to update forward-looking statements at some point in the future, we specifically disclaim any obligation to do so, even if our views change.
COVID-19
As

TRENDS AND UNCERTAINTIES

During fiscal 2023, we closely monitorexperienced higher than normal input cost inflation, including increases in certain raw materials, labor costs and supply chain pressure that negatively impacted operating results. Pricing actions taken during fiscal 2022 and 2023 mitigated some, but not all, of the

COVID-19
pandemic, inflationary pressures on the business. Ongoing inflation also could have an impact on our top priority remains protecting the healthcustomer’s purchasing decisions and safety of our employees, their families, and those in our communities. While essential operations continue in our locations around the world, many of our
non-manufacturing
employeesorder patterns. We estimate inflation will continue to work remotelyaffect us in fiscal year 2024, although at a decreasing rate compared to the prior two fiscal years.

Although we have no operations in or direct exposure to Russia, Belarus and travel remains limited. Safety guidelinesUkraine, we have experienced intermittent shortages in materials and procedures, including social distancingincreased costs for transportation, energy and enhanced cleaning,raw materials due, in part, to the negative impact of the Russia-Ukraine military conflict, which began in February 2022, on the global economy. Our European operations and customer base have been developed for

on-site
employees and these policies are regularly monitored and updatedadversely impacted by the conflict. As the conflict continues or worsens, it may further impact our internal Emergency Response Team.
Inbusiness, financial condition or results of operations during fiscal 2021,year 2024.

While the

impact of the COVID-19
global pandemic was more modest in fiscal 2023, it continued to impact our business operations and financial results. There has been a positive impactresults, particularly in salesthe first half of our biosecurity product lines, as the pandemic has created increased demand for these products, and sales into companion animal markets have benefitted, as remote work and stay at home orders have driven increased pet ownership.fiscal year in Asia. A number of our food safety diagnostic product lines have beenwere negatively impacted due to decreased demand in many of our customers’ businesses, particularly those serving restaurants, bars and other institutional food service markets; supply chain difficulties including vendor disruptions, border closures, shipping issues and labor shortages. Broadly speaking, many of our markets have recovered or are recovering from the pandemic, as supply chain difficulties and shipping issues;costs have decreased. A renewed outbreak of COVID-19 could result in further uncertainty and restricted travel, which hinders our ability to connect with customers. Duringbusiness disruptions. However, the current fiscal year, we have incurred less expense for travel, meals, trade showstrend is positive and some other customer-facing marketing activities; higher spend on shipping, cleaning activitiesnegative impacts appear to be moderating.

Overall, the impact of inflation, the Russia-Ukraine military conflict and personal protective equipment has somewhat offsetCOVID-19 remains uncertain. We continue to evaluate the nature and extent to which these savings.issues impact our business, including supply chain, labor availability and attrition, consolidated results of operations, financial condition and liquidity. We expect the

COVID-19
pandemic willthese issues to continue to impact our business operations and financial results through the majority of our 2022us throughout fiscal year.
year 2024.

CRITICAL ACCOUNTING POLICIES AND ESTIMATES

The discussion and analysis of our financial condition and results of operations are based on the consolidated financial statements that have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of these financial statements requires that management make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an ongoing basis, management evaluates the estimates, including but not limited to, those related to receivable allowances, inventories and intangible assets. These estimates are based on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Though the impact of the

COVID-19
pandemic to our business and operating results presents additional uncertainty, we continue to use the best information available to inform our critical accounting estimates. Actual results may differ from these estimates under different assumptions or conditions.

The following critical accounting policy reflectsestimates reflect management’s more significant judgments and estimates used in the preparation of the consolidated financial statements.

32


Income Taxes

We account for income taxes using the asset and liability method. Under this method, deferred income tax assets and liabilities are determined based on differences between the financial reporting and tax bases of assets and liabilities and for tax credit carryforwards and are measured using the enacted tax rates in effect for the years in which the differences are expected to reverse. Deferred income tax expense represents the change in net deferred income tax assets and liabilities during the year. The determination of income subject to income tax in each tax paying jurisdiction requires us to apply transfer pricing guidelines for certain intercompany transactions.

Our tax rate is subject to adjustment over the balance of the year due to, among other things, income tax rate changes by governments; the jurisdictions in which our profits are determined to be earned and taxed; changes in the valuation of our deferred tax assets and liabilities; adjustments to our interpretation of transfer pricing standards; changes in available tax credits or other incentives; changes in stock-based compensation expense; changes in tax laws or the interpretation of such tax laws; and changes in U.S. generally accepted accounting principles.

25

Table of Contents

Although we believe our tax estimates are reasonable and we prepare our tax filings in accordance with all applicable tax laws, the final determination with respect to any audit, and any related litigation, could be materially different from our estimates or from our historical income tax provisions and accruals. The results of an audit or litigation could have a material effect on operating results and/or cash flows in the periods for which that determination is made. In addition, future period earnings may be adversely impacted by litigation costs, settlements, penalties, and/or interest assessments.

Our wholly owned

As of May 31, 2023, the Company has approximately $153 million of undistributed earnings in its foreign subsidiaries. Approximately $41 million of these earnings are no longer considered permanently reinvested. The incremental tax cost to repatriate these earnings to the U.S. is immaterial. The Company has not provided deferred taxes on approximately $112 million of undistributed earnings from non-U.S. subsidiaries as of May 31, 2023 which are comprised of Neogen Europe, Quat-Chem Ltd, Megazyme Ltd, Megazyme IP, Neogen Italia S.r.l., Neogen do Brasil, Rogama Industria e Comercio Ltda, Neogen Latinoamérica, Neogen Argentina, Neogen Uruguay, Neogen Chile SpA, Neogen

Bio-Scientific
Technology Co (Shanghai), Neogen Food and Animal Security (India), Neogen Canada and Neogen Australasia Pty Limited.indefinitely reinvested in operations. Based on historical experience, as well as management’s future plans, earnings from these subsidiaries are expectedwill continue to be
re-invested
indefinitely for future expansion and working capital needs. Furthermore, our domestic operations have historically produced sufficient operating cash flow to mitigate the need to remit foreign earnings. On an annual basis, we evaluate the current business environment and whether any new events or other external changes might require a
re-evaluation
future evaluation of the decision to indefinitely
re-invest
these foreign earnings. It is not practicablepractical to determine the income tax liability that would be payable if such earnings were not reinvested indefinitely.
26

Table

Additionally, the company has elected to treat Global Intangible Low Tax Income (“GILTI”), as a period cost, and therefore, has not recognized deferred taxes for basis differences that may reverse as GILTI tax in future years.

Business Combinations and Customer Relationships Intangibles

We utilize the acquisition method of Contents

accounting for business combinations. This method requires, among other things, that results of operations of acquired companies are included in Neogen’s results of operations beginning on the respective acquisition dates and that assets acquired and liabilities assumed are recognized at fair value as of the acquisition date. Any excess of the fair value of consideration transferred over the fair values of the net assets acquired is recognized as goodwill.

As described in Note 3 "Business Combinations" to the consolidated financial statements, on September 1, 2022, we completed a transaction combining 3M’s food safety division with Neogen in a Reverse Morris Trust transaction for consideration of approximately $3.2 billion, which resulted in recording of a customer relationships intangible assets valued at $1.17 billion. We determined the fair value of the acquired customer relationships intangible assets by applying the multi-period excess earnings method, which involved the use of significant estimates and assumptions related to forecasted revenue growth rate and customer attrition rate. Valuation specialists were used to develop and evaluate the appropriateness of the multi-period excess earnings method, our discount rates, our attrition rate and our fair value estimates using our cash flow projections.

The fair value of assets acquired and liabilities assumed in certain cases may be subject to revision based on the final determination of fair value during a period of time not to exceed 12 months from the acquisition date. Legal costs, due diligence costs, business valuation costs and all other business acquisition costs are expensed when incurred.

33


Our estimates of fair value are based on assumptions believed to be reasonable at that time. If we made different estimates or judgments, it could result in material differences in the fair values of the net assets acquired.

Goodwill

We record goodwill when the purchase price of acquired businesses exceeds the value of their identifiable net tangible and intangible assets acquired. We periodically evaluate goodwill for impairment in accordance with the accounting guidance for goodwill and other indefinite-lived intangibles that are not amortized. We review our goodwill for impairment annually during the fourth quarter. In addition, we review goodwill for impairment whenever adverse events or changes in circumstances indicate a possible impairment.

This review is performed at the reporting unit level, and involves a comparison of the fair value of the reporting unit with its carrying amount, including goodwill. If the fair value of the reporting unit exceeds its carrying amount, goodwill of the reporting unit is not considered impaired. If the carrying amount of the reporting unit exceeds its fair value, an impairment loss is recognized in an amount equal to the excess carrying value over fair value.

In performing goodwill impairment testing, we utilize a third-party valuation specialist to assist management in determining the fair value of our reporting units. Fair value of each reporting unit is estimated based on a combination of discounted cash flows and the use of pricing multiples derived from an analysis of comparable public companies multiplied against historical and/or anticipated financial metrics of each reporting unit. These calculations contain uncertainties as they require management to make assumptions including, but not limited to, market comparables, future cash flows of the reporting units, and appropriate discount and long-term growth rates.

During fiscal year 2023, our business was organized into two reporting units: Food Safety and Animal Safety. The determination of our reporting units and impairment indicators also require us to make significant judgments.

As a result of our test in the fourth quarter of fiscal year 2023, we determined that the fair value of our reporting units exceeded their respective carrying values. As such, the annual impairment analysis resulted in no impairment in fiscal year 2023.

34


RESULTS OF OPERATIONS

Executive Overview
Consolidated revenues were $468.5 million

Historical Periods

Refer to Part II - Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations in our Form 10-K for the fiscal 2021, an increaseyear ended May 31, 2022 for discussion of 12% compared to $418.2 million in fiscal 2020. Organic sales overall increased 9%the Results of Operations, Segment Results of Operations, and Financial Condition and Liquidity for the year ended May 31, 2022 compared to the prior year.

year ended May 31, 2021, which is incorporated by reference herein.

Executive Overview

 

 

Year Ended

 

(in thousands, except earnings per share)

 

May 31, 2023

 

 

May 31, 2022

 

 

% Change

 

Consolidated

 

 

 

 

 

 

 

 

 

Revenues, net

 

$

822,447

 

 

$

527,159

 

 

 

56

%

Core Sales Growth

 

 

 

 

 

 

 

 

4

%

Food Safety

 

 

 

 

 

 

 

 

 

Revenues, net

 

$

546,797

 

 

$

259,979

 

 

 

110

%

Core Sales Growth

 

 

 

 

 

 

 

 

6

%

Animal Safety

 

 

 

 

 

 

 

 

 

Revenues, net

 

$

275,650

 

 

$

267,180

 

 

 

3

%

Core Sales Growth

 

 

 

 

 

 

 

 

2

%

% of International Sales

 

 

48

%

 

 

40

%

 

 

 

Effective Tax Rate

 

 

(3.8

)%

 

 

19.8

%

 

 

 

Net Income

 

$

(22,870

)

 

$

48,307

 

 

 

-147

%

Earnings per Diluted Share

 

$

(0.12

)

 

$

0.45

 

 

 

 

Cash from Operations

 

$

41,028

 

 

$

68,038

 

 

 

 

Food Safety segmentfiscal year 2023 core sales were $234.2 million in fiscal 2021 compared to $212.7 million in fiscal 2020, an increase of 10%. Organic sales increased 6%, while the purchase of four former distributors and a small manufacturer (Abtek) in fiscal 2020 and the December 2020 acquisition of Megazyme contributed $8.0 million in revenues.
Animal Safety segment sales were $234.2 million in fiscal 2021, an increase of 14% compared to $205.5 million in fiscal 2020. Organic sales rose 13%, withexclude revenues from the acquisitions of Cell BioSciences,Corvium (February 2023), 3M FSD (September 2022), Thai-Neo Biotech (July 2022), and Delf/Abbott Analytical (November 2021) and also excludes the impact of changes in fiscal 2020, and StandGuard, in July 2020, contributing the remaindercurrency rates.
Food Safety revenues include $279.5 million from 3M FSD, which we combined with on September 1, 2022. All of the growth.
global revenue from this business is reported within the Food Safety segment.
Animal Safety fiscal year 2023 core sales exclude revenues from the acquisitions of Genetic Veterinary Sciences (December 2021) and CAPInnoVet (September 2021) and also excludes the impact of changes in currency rates.

International sales were 39.1% of total sales in fiscal 2021 compared to 39.4% of total sales in fiscal 2020.

Our effective tax rate was 19.1% in fiscal 2021 compared to an effective tax rate of 17.7% in fiscal 2020.
Net income was $60.9 million, or $0.57 per diluted share, an increase of 2% compared to $59.5 million, or $0.56 per share, in the prior year.
Cash generated from operating activities in fiscal 2021 was $81.2 million, compared to $85.9 million in fiscal 2020.
Revenue

Neogen’s international revenues were $183.2$398.4 million in fiscal 2021,year 2023, compared to $164.7$209.3 million in fiscal 2020. Currency translation had a negligible impact on2022, an increase of 90%. Revenues from 3M FSD drove the international sales increase. Since September 1, 2022, 67% of 3M FSD revenues for the full year, with gains in the U.K., Italy, China, Australia and Canada almost entirely offset by negative impact in Brazil, Mexico and Argentina. In a neutral currency environment,were international sales, would have been $3.4 million higher than reported in the first nine months of fiscal 2021. However, the Brazilian real and Mexican peso strengthened significantly in the fourth quarter, resulting in an overall positive effectcompared to Neogen’s historical average of approximately $3.3 million from currency translations; the full year impact from currency translations was minimal.

Sales results40%.

35


Revenue changes, expressed in percentages, for fiscal 20212023 compared to the prior year are as follows for the legacy business at each of our international locations:

   
Revenue
  
Revenue
 
   
Change
  
Change
 
   
USD
  
Local Currency
 
UK Operations
   10  4
Brazil Operations
   (8%)   15
Neogen Latinoamerica
   9  13
Neogen China
   101  89
Neogen India
   4  7
Neogen Australasia
   78  61
Neogen Canada
   14  9
The revenue increase

 

Revenue
Change
USD

 

 

Revenue
Change
Local Currency

 

U.K. Operations (including Neogen Italia)

 

 

(3

)%

 

 

9

%

Megazyme

 

 

(3

)%

 

 

6

%

Brazil Operations

 

 

11

%

 

 

10

%

Neogen Latinoamerica

 

 

10

%

 

 

4

%

Neogen Argentina

 

 

(5

)%

 

 

48

%

Neogen Uruguay

 

 

(1

)%

 

 

(9

)%

Neogen Chile

 

 

16

%

 

 

24

%

Neogen China

 

 

(11

)%

 

 

(4

)%

Neogen India

 

 

2

%

 

 

11

%

Neogen Canada

 

 

(6

)%

 

 

0

%

Neogen Australasia

 

 

3

%

 

 

11

%

Excluding the December 2021 acquisition of Delf, sales at our U.K. operations increased 5% in U.S. dollars at Neogen Europelocal currency, which was led by a 22% increaseincreased sample volume in the pig and poultry markets. In local currency, revenue in Brazil increased 10% in fiscal 2023, driven by strong sales of disinfectantthe company’s natural toxin test kits, including tests to detect aflatoxin in corn, as well as increases in insect and veterinaryrodent control products, and genomics testing. In local currency, Neogen Latinoamerica revenues rose by 4% in fiscal 2023, led by our diagnostic testing portfolio and culture media.

China’s revenue decreased 4% in local currency, which was primarily due to

COVID-19
related salesthe result of hand sanitizer and disinfectant in the U.K.COVID-19 lockdowns in the first quarter and strong cleaner and disinfectant sales throughouthalf of the entire year to Asia to mitigate the impact of African Swine Fever. Partially offsetting this growth were lower sales of diagnostic test kits due to
COVID-19
shutdowns; additionally, a large portion of sales into European Union countries from January through May were sold through our Neogen Italia subsidiary as Brexit created export issues from the U.K.
Revenues in Brazil decreased 8% in USD in fiscal 2021 but increased 15% in local currency, as the Brazilian real devalued significantly against the U.S. dollar during the year. In local currency, revenue at Neogen Australasia increased 11% in fiscal 2023, led by increased sales of our diagnostic test kits increased 10%, genomics revenues increased 19%, due to new business in the beef market, and insecticides revenues grew 22%, partially the result of a large tender sale. Neogen Latinoamerica grew revenues by 9% in USD, with growth in biosecurity products, veterinary instruments and diagnostic test kits. China’s sales approximately doubled, from growth in biosecurity products and genomicsbovine genomic services. Neogen Australasia benefitted from the February 2020 acquisition of a food safety distributor; organic sales increased 59% at this location in fiscal 2021, from strength in genomics services for the companion animal and bovine markets and increased market share of food safety diagnostic test kits.
27

Table of Contents

Service Revenue

Service revenue, which consists primarily of genomics services sales to animal protein and companion animal markets, was $92.2$107.4 million in fiscal 2021,2023, an increase of 12%5% over prior fiscal year sales of $82.6$102.5 million. The increase was primarily driven by growth was led by increases in sample volumes from the globalU.S. beef and companion animal markets for genomics testing and commercial beefhigher sales of our Neogen Analytics software as a service (SaaS) product. These increases were partially offset by COVID-related shutdowns in China in the first half of fiscal 2023 and lower genomics sales to the U.S. porcine and poultry markets, and the Chinese porcine market, as that country has begun recovery from its African swine fever outbreak.

two significant customer shifted to lower-cost competitors.

REVENUES

   
Year Ended
 
(dollars in thousands)
  
May 31, 2021
   
Change
  
May 31, 2020
   
Change
  
May 31, 2019
 
Food Safety:
        
Natural Toxins, Allergens & Drug Residues
  $76,614    1 $76,207    (3%)  $78,373 
Bacterial & General Sanitation
   44,009    5  41,780    (0%)   41,966 
Culture Media & Other
   56,922    19  47,847    (4%)   49,857 
Rodenticides, Insecticides & Disinfectants
   36,542    26  28,890    13  25,584 
Genomics Services
   20,157    12  17,967    2  17,694 
  
 
 
    
 
 
    
 
 
 
  $234,244    10 $212,691    (0%)  $213,474 
Animal Safety:
        
Life Sciences
   5,715    (10%)   6,322    (20%)   7,858 
Veterinary Instruments & Disposables
   48,128    12  42,941    (4%)   44,582 
Animal Care & Other
   35,897    26  28,389    (5%)   29,941 
Rodenticides, Insecticides & Disinfectants
   77,458    13  68,815    4  66,389 
Genomics Services
   67,017    14  59,012    14  51,942 
  
 
 
    
 
 
    
 
 
 
  $234,215    14 $205,479    2 $200,712 
  
 
 
    
 
 
    
 
 
 
Total Revenue
  $468,459    12 $418,170    1 $414,186 
  
 
 
    
 
 
    
 
 
 

 

Year Ended

 

(dollars in thousands)

 

May 31, 2023

 

 

May 31, 2022

 

 

% Change

 

Food Safety:

 

 

 

 

 

 

 

 

 

Natural Toxins, Allergens & Drug Residues

 

$

82,567

 

 

$

79,395

 

 

 

4

%

Bacterial & General Sanitation

 

 

134,934

 

 

 

47,282

 

 

 

185

%

Culture Media & Other

 

 

267,178

 

 

 

75,278

 

 

 

255

%

Rodent Control, Insect Control & Disinfectants

 

 

39,655

 

 

 

35,691

 

 

 

11

%

Genomics Services

 

 

22,463

 

 

 

22,333

 

 

 

1

%

 

$

546,797

 

 

$

259,979

 

 

 

110

%

Animal Safety:

 

 

 

 

 

 

 

 

 

Life Sciences

 

 

6,254

 

 

 

5,685

 

 

 

10

%

Veterinary Instruments & Disposables

 

 

63,843

 

 

 

63,938

 

 

 

0

%

Animal Care & Other

 

 

39,068

 

 

 

39,805

 

 

 

(2

)%

Rodent Control, Insect Control & Disinfectants

 

 

87,423

 

 

 

83,610

 

 

 

5

%

Genomics Services

 

 

79,062

 

 

 

74,142

 

 

 

7

%

 

$

275,650

 

 

$

267,180

 

 

 

3

%

Total Revenue, net

 

$

822,447

 

 

$

527,159

 

 

 

56

%

36


Year Ended May 31, 20212023 Compared to Year Ended May 31, 2020

2022

Food Safety:

The
COVID-19
pandemic, which began in the second half of fiscal 2020, continued to cause difficult operating conditions in many of our key market segments in fiscal 2021. Shelter in place orders across the U.S. and in most of our international markets, the closure or reduced output of businesses due to quarantine and/or local legislation, disruption in the supply chain resulting from reduction in
end-market
demand and shipping issues, and the inability of some markets to react quickly to these changes, each disrupted our revenues.

Natural Toxins, Allergens

& Drug Residues –
SalesRevenues in this category increased 1%4% in fiscal 2021, with a 6% increase in2023. Excluding sales of natural toxin test kits and a 5% increase in our allergensthe acquired allergen product line partially offset byfrom 3M FSD, sales in this category decreased 3% due to a 30% decreaselarge decline in sales of drug residue test kits. Sales of drug residue test kits have continued to decline as we ended an exclusive distributor agreementthat were largely discontinued in Europe and faced competitive pressure and lower demand due to poor economic conditions.
fiscal 2023.

Bacterial

& General Sanitation –
Sales in this category increased 5%185% in fiscal 20212023 compared to the prior fiscal year. SalesExcluding the contribution of the Clean-Trace® line of general sanitation products to detect spoilage organismsand the pathogen test kit product line, both acquired from 3M FSD, organic sales in processed foods increased 19%this category were flat for the full year. A 3% increase in fiscal 2021, resulting from sales of our new instrument (Soleris NG), which launchedSoleris line of spoilage detection consumables was offset by a decline in the first quarter, and increased consumables sales from new instrument placements. Sales of our AccuPoint line of general sanitation monitoring product line were flat as many customers were shut down or operating at reduced capacityproducts, primarily caused by lack of supply of critical components for a portion of the year, resulting in use of less consumables. A next generation reader for this product line was launched late in the fourth quarter; there will be significant sales and marketing focus on this product line in fiscal 2022. Sales of test kits to detect pathogens decreased 2%, as lower sales of ANSR equipment were only partially offset by increases from our
Listeria
Right Now test kit, which grew 21% in fiscal 2021.
28

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reader.

Culture Media

& Other –
Sales in this category increased 19%255% in fiscal 20212023 compared to the prior fiscal 2020.year, driven primarily from revenues resulting from 3M FSD. Excluding sales fromof the December 2020 acquisitionPetrifilm indicator organism and sample handling product lines acquired in the Transaction, sales rose 7% for the year. Culture media revenues rose 13%, primarily due to a large custom order in the third quarter of Megazyme, sales increased 8%. This category includesthe year. Additionally, sales of acquired inventory of
non-Neogen
manufactured products from our new businesses in Italy andNeogen Analytics software as a service platform increased significantly during the South American southern cone countries; these sales are not expected to continue long-term. Sales of Neogen Culture Media increased 1% as new business gained in the U.S. from a
COVID-19
vaccine manufacturer offset the loss of some business due to competitor pricing.
Rodenticides, Insecticides
year, with approximately 250 sites now on contract.

Rodent Control, Insect Control & Disinfectants –

RevenuesSales of products in this category sold through our Food Safety operations increased 26%11% in fiscal 20212023 compared to the prior fiscal 2020, due primarily to continued strength inyear. Excluding the November 2021 acquisition of Delf, the increase was 4%, led by higher sales of cleaners and disinfectant salesdisinfectants in China resulting from increased demand due to the African swine fever outbreak in that country and the
COVID-19
pandemic. We also benefitted from strong sales of hand and skin sanitizing products at our U.K.-based Quat-Chem location in the first quarter of this fiscal year.
China.

Genomics Services –

Sales of genomics services sold through our Food Safety operations increased 12%1% in fiscal 20212023 compared to the prior fiscal year, with increases in beef business in Brazil and the U.K. partially offset by a decline in sample volumes in China, as the first half of the fiscal year was negatively impacted by COVID-19 shutdowns.

Animal Safety:

Life Sciences – Sales in this category increased 10% in fiscal 2023 compared to the prior fiscal year, primarily due to higher salesdemand from customers purchasing substrates and reagents used in the Chinese porcine and bovine markets.

Animal Safety:
Life Sciencesclinical diagnostic test kits.

Veterinary Instruments & Disposables

Sales in this category decreased 10%were flat in fiscal 20212023 compared to the same periodprior fiscal year, as significant increases in cohesive wrap business won in the second half of the year were offset by lower sales of veterinary instruments, reflecting difficult comparisons to large stocking orders of needles and syringes in the prior year primarily the result of lower forensic drug test kit sales to large commercial labsfrom new business earned in the U.S. as the
COVID-19
pandemic created less demand for testing; a reduction in sales of products to the U.S. horse racing industry in the U.S. also contributed to the decline, as racing activity was down.
Veterinary Instruments
 & Disposables –
Revenues in this category increased 12% in fiscal 2021 compared to fiscal 2020. Veterinary instruments sales increased 16% for the year, led by increases in detectable needles and syringes as we gained new customers and benefitted from increased demand resulting from higher numbers of production animals in existing markets. Partially offsetting this increase was a 9% decline in protective wear sales, as gloves were on backorder for much of the current year due to COVID related demand.
that period.

Animal Care

& Other –
Sales of these products increased 26%decreased 2% in fiscal 20212023 compared to the prior fiscal 2020; this category includesyear. Lower sales of food safety products sold through our Australian operation, the result of a February 2020 acquisition of a distributor. Excluding these sales, revenues in this category increased 21%. Sales of our small animal supplements, vitamin injectables and joint pain products benefitted from growth in veterinary markets, as the
COVID-19
pandemic has led to an increase in pet ownership, particularly dogs and cats. Additionally, sales rose for our equine supplements and antibiotics, primarily due to strong demand in these markets. This category also includes sales of our thyroid treatment for dogs, which became available for sale late in the fourth quarter. Partially offsetting these gains wassupply constraints, more than offset a 49% decline7% increase in sales of dairy supplies due to the June 2020 terminationvaccines and biologics products and a 4% increase in sales of an agreement in which we distributed these products for a large manufacturer of dairy equipment.
Rodenticides, Insecticides
small animal supplements.

Rodent Control, Insect Control & Disinfectants –

Sales in this category increased 13%5% in fiscal 2021,2023, compared to the prior fiscal year. Rodenticide sales increased 42% as rodent pressure in certain areas of the U.S. increased significantly. Insecticide sales rose 15%, due in part to our acquisition of the StandGuard product line for fly control on July 31, 2020; organic sales in this category increased 7%. CleanersCleaner and disinfectants sales decreased 15% resulting from lowerrose 11% on new business earned, insect control product sales of water treatment productsincreased 6%, and the transfer of a product linerodenticide revenues increased 1%, each compared to our U.K. operation; additionally, opportunistic sales of sanitizing products in the fourth quarter of the prior year, due to extremely high demand early in the
COVID-19
pandemic, did not continue at those levels in fiscal 2021.
year.

Genomics Services –

Sales in this category increased 14%7% in fiscal 20212023 compared to the prior fiscal 2020. Theyear. Excluding the December 2021 acquisition of Genetic Veterinary Sciences, the growth was 2%. Growth was led by strong increases to the U.S. and Australian companion animal markets, driven by increased pet adoption and higher consumer spending on pets during the
COVID-19
pandemic. Gains in the commercial beef and beef association marketsdairy cattle testing in the U.S., Canada and Australia, also contributed to the growth, as well as the recent launch of a new high-density chip for white leg shrimp.
Year Ended May 31, 2020 Compared to Year Ended May 31, 2019
Food Safety:
The
COVID-19
pandemicand strength in the second half of fiscal 2020 resulted in difficult operating conditions in many of our key market segments. Shelter in place orders across the U.S. and in a number of our international markets, the closure or reduced output of businesses due to quarantine, disruption in the supply chain resulting from reduction in
end-market
demand, and the inability of some markets to react quickly to these changes, each adversely impacted ourdomestic companion animal revenues.
29

Table of Contents
Natural Toxins, Allergens
 & Drug Residues –
Sales in this category These increases were 3% lower in fiscal 2020 compared to the prior year, driven by a 30% decline in sales of drug residues test kits, due to lower demand from a large distributor in Europe. In January 2020, we ended our exclusive relationship with this distributor and have begun marketing these products directly into the European market. Partially offsetting the decrease in drug residue testing, the natural toxins and allergens product lines each increased 4% for the year. The natural toxin increase was due to continued new business earned in Brazil for aflatoxin and DON test kits, partially offset by declines in porcine and poultry testing revenues, due to the loss of two large customer to lower cost competitors.

37


GROSS MARGIN

Gross margin, expressed as a percentage of sales, of DON test kits in the U.S. and France, the result of mild outbreaks inwas 49.4% during fiscal year 2023 compared to 46.1% during the prior fiscal year. The increase was primarily due to the incremental revenues from the 3M FSD merger, which generated gross margin higher than the legacy company average margin. Within each reporting segment, increased raw material costs pressured gross margins in certain product lines. However, freight costs declined significantly during the comparative period particularly benefitting the Animal Safety segment, although they remained higher than pre-pandemic levels in some areas. Pricing actions taken during the year which did not recur inalso mitigated the impact of cost increases.

OPERATING EXPENSES

(dollars in thousands)

 

2023

 

 

2022

 

 

% Change

 

Sales and Marketing

 

$

141,222

 

 

$

84,604

 

 

 

67

%

General and Administrative

 

 

201,179

 

 

 

82,742

 

 

 

143

%

Research and Development

 

 

26,039

 

 

 

17,049

 

 

 

53

%

Total Operating Expense

 

$

368,440

 

 

$

184,395

 

 

 

100

%

Operating expenses were $368.4 million during fiscal 2020.year 2023, compared to $184.4 million during the prior fiscal year. The allergen test kit increase was primarily the result of strong gliadin, milk$58.2 million of legal, consulting and coconut allergen test kit salesother expenses related to the 3M FSD transaction and incremental ongoing expenses resulting from the employees who conveyed over to Neogen from 3M FSD and the amortization of intangible assets acquired in the U.S. market, although fourth quarter sales declined 7% due to lower business with customers supplying restaurantsTransaction.

Sales and other food service organizations, whichMarketing:

Sales and marketing expenses were adversely impacted by

COVID-19.
Bacterial
 & General Sanitation –
Sales in this category were essentially flat in$141.2 million during fiscal 2020year 2023, compared to $84.6 million during the prior fiscal year. SalesThe increase in expense was due primarily to $45.4 million in costs incurred for the 3M FSD business, primarily consisting of test kitscompensation and related expenses for the conveying 3M FSD sales and marketing team, and the charges for transition services provided by 3M FSD. These invoicing and distribution services will be provided under contract for a period of up to detect pathogens decreased 2%, as lower sales18 months, concluding by March 1, 2024. The remainder of ANSR equipment were only partially offset by increases from our
Listeria
Right Now test kit, which grew 24% in fiscal 2020. Sales of our AccuPoint sanitation monitoring product line increased 6%, on increases in both readers and samplers. Sales of products to detect spoilage organisms in foods decreased 7% in fiscal 2020 on reduced sales of readers and consumable vialsthe increase during the year was due primarily to higher personnel related spending in the legacy business, the result of headcount additions and compensation increases. In addition, travel, trade shows and other customer facing activities continued to increase during the year with the easing of COVID-19 restrictions and greater willingness by customers to interact.

General and Administrative:

General and administrative expenses were $201.2 million during fiscal year 2023, compared to $82.7 million during the prior fiscal year. The current fiscal year included $58.2 million in transaction fees and integration expenses resulting from lower market demandthe 3M FSD transaction and customer losses.

Culture Media
 & Other –
Sales$60.9 million in this category decreased 4% in fiscal 2020 compared to fiscal 2019. This category includes forensic drug test kits sold within Brazil, which declined significantly as a large commercial lab customer in that country moved to an alternative new technology which provided higher throughput. Culture media revenues declined 5%, due to lower end market demand from several large customersamortization of intangible assets acquired in the U.S. Higher shipping revenues, which rose 12%Transaction. Remaining increases for the year and lower rebates offered to certain customers, both of which are reported in this category, partially offset the lower forensic and culture media revenues.
Rodenticides, Insecticides
 & Disinfectants –
Revenues of products in this category sold through our Food Safety operations increased 13% in fiscal 2020 compared to fiscal 2019. This category was led by increases in sales of cleaners and disinfectants to customers in Europe, the Middle East and China, partially offset by a decrease in sales of rodenticides in Central America due to lower demand from a large distributor, and reduced demand of cleaners and disinfectants in India, due to a large order in 2019 which did not recur in fiscal 2020.
Genomics Services –
Sales of genomics services sold through our Food Safety operations increased 2% in fiscal 2020 compared to the prior year, primarily due to higher sales in the European bovine and equine markets. Partially offsetting this increase were lower revenues from our genomics operation in Brazil due to a research project with the Brazilian government from 2019 which did not recur in fiscal 2020.
Animal Safety:
A significant proportion of the Animal Safety products are marketed and sold through our veterinary distributor network; this channel was impacted in both fiscal years 2019 and 2020, as difficult market conditions resulting from increased tariffs and political uncertainties in our agricultural and animal protein markets continued. The
COVID-19
pandemic in the second half of fiscal 2020 has exacerbated these market conditions; further, the market uncertainty resulting from
COVID-19
has caused our larger distributor partners to implement working capital improvement programs by lowering inventory levels which resulted in lower sales of many products in our animal health portfolio. Partially offsetting this weakness in the fourth quarter were higher sales of several of our cleaning and disinfecting products due to demand caused by the
COVID-19
pandemic.
Life Sciences –
Sales in this category decreased 20% in fiscal 2020 compared to the same period in the prior year, the result of lower forensic drug test kit sales to a large commercial lab in the U.S. serving the Brazilian market, a reduction in sales of products to the U.S. horse racing industry in the U.S. due to a decline in domestic racing activity, and the consolidation of several state laboratories.
Veterinary Instruments
 & Disposables –
Revenues in this category decreased 4% in fiscal 2020 compared to fiscal 2019. Veterinary instruments sales were down 7% for the year, primarily the result of a 20% decline in needlesadditional personnel hired to accommodate the increased size and 3% decline in syringes, due to lower demand from our largest distributors. Partially offsetting these decreases, protective wearcomplexity of the organization, compensation increases across the organization, the issuance of share based compensation grants, software license fees and consumables increased 24% for theother information technology infrastructure investments. Fiscal year on the strength2022 included $25.6 million of a $956,000 increase in gloves in the fourth quarter of fiscal 2020, the result of demand caused by the
COVID-19
pandemic.
Animal Care
 & Other –
Sales of these products decreased 5%3M FSD-related transaction fees.

Research and Development:

Research and development expense was $26.0 million in fiscal 2020year 2023, compared to fiscal 2019. Antibiotics and injectable vitamin products were down 20% and 15%, respectively, due primarily to inventory destocking at distributors. Sales of our biologics product line, marketed primarily into$17.0 million during the equine market, declined 17%, and our equine supplements were also down 20%, due to lower demand from end customers in this market. Sales of wound care products rose 9% to partially offset these losses.

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Table of Contents
Rodenticides, Insecticides
 & Disinfectants –
Sales in this category increased 4% inprior fiscal 2020, compared to the prior year. The increase was due primarily the result of $8.4 million of ongoing costs associated with the conveying 3M FSD employees.

OPERATING INCOME

Operating income was $37.5 million during fiscal year 2023, compared to a $2.6operating income of $58.6 million increase in sales of cleaners and disinfectants for the year, driven in large part by growth in hand sanitizers, disinfectants, and disinfecting wipes in the fourth quarter resulting from the

COVID-19
pandemic. Revenues for water disinfection in animal protein production environments rose 8% overprior fiscal 2019. Rodenticide sales increased 1% over the prior year, as strong growth in the retail market was almost entirely offset by lower sales to agricultural markets in the northwest U.S., due to lower rodent pressure. Insecticide revenues declined 2% for the year.
Genomics Services –
Sales in this category increased 14% in fiscal 2020, aided by the acquisition of Livestock Genetics (September 2018) and Delta Genomics (January 2019); organic growth in this category was 12%. Strong growth in the companion animal and commercial beef cattle markets was partially offset by revenue decreases in the U.S. commercial dairy market due to weak economic conditions in that market, resulting from a movement away from dairy milk towards alternative products.
COST OF REVENUES
(in thousands)
  
2021
   
Change
  
2020
   
Change
  
2019
 
Cost of Revenues
  $253,403    14 $221,891    0 $222,266 
Cost of revenues increased 14% in fiscal 2021 compared to fiscal 2020 and was essentially flat in fiscal 2020 compared to fiscal 2019. This compares with revenue increases of 12% in fiscal 2021 and 1% in fiscal 2020. Expressed as a percentage of sales, costoperating income was 4.6% during fiscal year 2023 and 11.1% during fiscal year 2022. Operating income, both in dollars and expressed as a percentage of revenues was 54.1%, 53.1% and 53.7% in fiscal years 2021, 2020 and 2019, respectively. Gross margins were 45.9%, 46.9%, and 46.3% for fiscal years 2021, 2020, and 2019, respectively.
Fiscal 2021
– Our overall gross marginsales, declined 100 basis points in fiscal 2021 as pressure on the worldwide supply chain caused by the
COVID-19
pandemic resulted in increased overhead costs; in particular, freight costs on inventory purchases increased 53% in fiscal 2021 compared to the prior year. Additional cost increases resulted from personnel costs, in part from the increased volumes, but also due to labor shortages, contracted services primarily related to our recently launched instruments, and higher health insurance costs domestically, as employees and their families utilized elective medical services postponed from the fourth quarter of fiscal 2020 due to
COVID-19.
To a lesser extent, the shift in mix within the Food Safety segment towards products with lower gross margins negatively impacted the consolidated gross margin percentage.
Fiscal 2020
– Our overall gross margin improved 60 basis points in fiscal 2020, primarily from improved gross margin in the Animal Safety segment and improved efficiencies, resulting from a focus on cost reductions in certain areas. These efforts resulted in a slight decrease in cost of revenues compared to the prior fiscal year.
Food Safety Gross Margins:
Food Safety gross margins were 49.2%, 51.4% and 51.8% in fiscal years 2021, 2020 and 2019, respectively.
Fiscal 2021 –
Food Safety margins decreased 220 basis points in fiscal 2021,year period primarily due to higher sales of equipment such as the Soleris NG, which was launched in the current year and has lower gross margins than our diagnostic test kits, and cleaners and disinfectants sold through our China location, which reports through the Food Safety segment. We were also negatively impacted by increased freight, labor and other overheadtransaction costs throughout the segment.
Fiscal 2020 –
Food Safety margins decreased 40 basis points in fiscal 2020, primarily due to lower sales of higher margin forensic test kits in Brazil, and the continued strength of the U.S. dollar against currencies in the countries in which we operate; our international operations pay for their inventory primarily in U.S. dollars. In a neutral currency environment, Food Safety segment sales would have been $5.4 million higher in fiscal 2020.
Animal Safety Gross Margins:
Animal Safety gross margins were 42.6%, 42.3% and 40.6% in fiscal years 2021, 2020 and 2019, respectively.
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Fiscal 2021 –
Animal Safety gross margins increased by 30 basis points, primarily from strong sales of higher margin rodenticide and companion animal products and cost efficiencies; somewhat offsetting these gains, gross margin in this segment was negatively impacted by higher freight costs as rates to bring product into inventory rose significantly during the year, from both domestic and international sources.
Fiscal 2020 –
Animal Safety gross margins increased by 170 basis points, driven by increased sales of higher margin disinfectant products, particularly in the fourth quarter of the year as a result of the
COVID-19
pandemic, which caused heavy demand for our sanitizing products. In addition, a mix shift towards genomics services for the companion animal markets, which have higher gross margins within the genomics business, contributed to the improvement.
OPERATING EXPENSES
(dollars in thousands)
  
2021
   
Change
  
2020
   
Change
  
2019
 
Sales and Marketing
  $73,443     5%  $69,675   (1%)  $70,230 
General and Administrative
   51,197   15%   44,331     9%   40,791 
Research and Development
   16,247   10%   14,750   15%   12,805 
  
 
 
     
 
 
     
 
 
 
Total Operating Expense
  $140,887     9%  $128,756     4%  $123,826 
  
 
 
     
 
 
     
 
 
 
Overall operating expenses increased by 9% in fiscal 2021 and 4% in fiscal 2020, each compared to the prior year. These increases compare to revenue increases of 12% and 1%, respectively, for each comparative period.
Sales and Marketing:
Sales and marketing expenses increased by 5% in fiscal 2021 compared to fiscal 2020 and decreased 1% in fiscal 2020 compared to the prior year. As a percentage of sales, sales and marketing expense was 15.7%, 16.7% and 17.0% in fiscal years 2021, 2020 and 2019, respectively.
Fiscal 2021
– The $3.8 million, or 5%, increase in sales and marketing expenses in fiscal 2021 resulted primarily from increases in employee compensation expenses such as salaries, bonuses, and commissions, reflecting the increase in sales for the year, as well as increased headcount as we returned to normal staffing levels. In addition, shipping costs rose in line with revenues, health insurance costs rose as employees and their families resumed receiving medical treatment and procedures which had been deferred in the fourth quarter of the prior fiscal year. Advertising and outside services also increased to support the launch of a number of new products during the year, most notably the Soleris NG and Accupoint NG readers. Partially offsetting these increases was $3 million in decreased spending for travel and meals and entertainment for the year, the result of travel restrictions and reductions in
face-to-face
sales activities in most of our markets for the majority of the year. Travel and in person customer meetings did begin to pick up in some geographic areas in the second half of fiscal 2021 as
COVID-19
restrictions were eased.
Fiscal 2020
– The $550,000 decline in sales and marketing expenses in fiscal 2020 was driven by a $1.3 million, or 7.4%, decline in spending in this category in the fourth quarter of the year, caused by a reduction in business travel, meals and entertainment, trade shows, and related marketing expenses, as the
COVID-19
global pandemic resulted in strict travel restrictions and reductions in face to face sales activities in many of our markets during the quarter. Partially offsetting these declines were higher compensation and related fringe benefits, the result of increased headcount, increased shipping expenses, and higher regulatory expense due to product registration efforts in our international markets.
General and Administrative:
General and administrative expenses rose 15% in fiscal 2021 compared to fiscal 2020 and by 9% in fiscal 2020 compared to fiscal 2019. As a percentage of sales, general and administrative expense was 10.9%, 10.6% and 9.8% in fiscal years 2021, 2020 and 2019, respectively.
Fiscal 2021 –
In fiscal 2021, we spent $3.1 million on strategic consulting, legal and other professional fees related to acquisition activity for businesses which we were ultimately not successful in acquiring. Excluding these costs, the increase in general and administrative expense in fiscal 2021 was 8%. Other increases in the current year included compensation increases due to increased headcount, including the addition of a number of senior management positions, incremental amortization expenses
(non-cash)
resulting from recent acquisitions, and higher levels of depreciation
(non-cash)
and related software and licensing costs from continued investments in information technology infrastructure and applications. Increases in this cost category resulting from the Megazyme acquisition totaled $957,000.
32

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Fiscal 2020 –
Higher stock-based compensation costs3M FSD transaction and a significant uptick in legal fees, driven in part from the number of acquisitions completed during the year, resulted in the overall 9% expense increase. In addition, the Company continued to invest in information technology infrastructure, network capabilities and
e-commerce
initiatives. This resulted in higher depreciation on
IT-related
hardware and increased license fees on software investments. These increases were somewhat offset by a reduction in outside consulting. General and administrative expenses at five new company locations, the result of acquisitions in the second half of fiscal 2020, totaled $520,000.
Research and Development:
Research and development expenses increased 10% in fiscal 2021 and 15% in fiscal 2020, each compared to the prior year. As a percentage of revenue, these expenses were 3.5% in fiscal year 2021, 3.5% in fiscal year 2020 and 3.1% in fiscal year 2019; we expect to spend between 3% and 4% of total revenue on research and development annually as we continue to make investments in our future growth.
Fiscal 2021 –
The 10% increase in research and development expenses in fiscal 2021 was primarily the result of increased compensation expense, resulting from scheduled annual increases and additional headcount from the Megazyme acquisition, project expense relating to new product innovation, spending with outside partners on the new readers launched in this fiscal year, and testing and approval costs for new product development.
Fiscal 2020 –
The 15% increase in research and development expenses in fiscal 2020 was primarily the result of continued spending with development partners for two new readers, launched in fiscal 2021. Increased compensation expense, resulting from investments in people as we heighten the development capabilitiesamortization of the group, higher depreciation expense from continued investment in analytical equipment, and an increase in contracted services also contributed to the expense growth.
OPERATINGintangible assets acquired.

38


OTHER (EXPENSE) INCOME

(dollars in thousands)
  
2021
   
Change
  
2020
   
Change
  
2019
 
Operating Income
  $ 74,169   10%  $ 67,523   (1%)  $ 68,094 
Our operating income rose 10% in fiscal 2021 compared to fiscal 2020 and decreased by 1% in fiscal 2020 compared to fiscal 2019. Expressed as a percentage of revenues, operating income was 15.8%, 16.1% and 16.4% in fiscal years 2021, 2020 and 2019, respectively.
Gross margins rose by $18.8 million, or 10% in fiscal 2021; this increase was partially offset by an increase of $12.1 million, or 9%, in operating expenses, resulting in a $6.6 million, or 10%, increase in operating income compared to fiscal 2020.
Gross margins rose by $4.4 million in fiscal 2020; the increase was more than offset by an overall increase of $4.9 million, or 4.0%, in operating expenses, resulting in a 1% decrease in operating income compared to fiscal 2019.
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OTHER INCOME (EXPENSE)

Other (Expense) Income (Expense) for the previous threetwo fiscal years consisted of the following:

(dollars in thousands)
  
2021
   
2020
   
2019
 
Interest income (net of expense)
  $1,614   $5,992   $4,683 
Foreign currency transactions
   (541   (1,178   (1,279
Royalty income
   —      1    150 
Licenses and settlements
   9    (38   672 
Quat-Chem contingent consideration
   —      —      422 
Deoxi contingent consideration
   —      —      (10
Magiar contingent consideration
   111    —      —   
Livestock Genomics contingent consideration
   37    —      —   
Other
   (131   5    227 
  
 
 
   
 
 
   
 
 
 
Total Other Income
  $1,099   $4,782   $4,865 
  
 
 
   
 
 
   
 
 
 

(dollars in thousands)

 

2023

 

 

2022

 

Interest income

 

$

3,166

 

 

$

1,339

 

Interest expense

 

 

(55,961

)

 

 

(72

)

Foreign currency transactions

 

 

(5,322

)

 

 

(40

)

Loss on sale of minority interest

 

 

(1,516

)

 

 

-

 

Loss on investment

 

 

(500

)

 

 

-

 

Contingent consideration adjustments

 

 

300

 

 

 

220

 

Other

 

 

276

 

 

 

142

 

Total Other Income

 

$

(59,557

)

 

$

1,589

 

The net interest expense recorded during fiscal year 2023 was the result of debt incurred to fund the 3M FSD transaction. In fiscal 2022, the Company had no debt outstanding. Interest income declined by $4.4 million in fiscal 2021 comparedrelates to fiscal 2020, despite higher cash andearnings on our marketable securities balances, asportfolio. Higher yields on fixed income securities declined significantly during the year; the U.S. Federal Reserve intervened in markets toportfolio were partially offset by lower rates to stimulate the economy during the

COVID-19
pandemic. Interest income rosebalances in fiscal year 2020 compared to fiscal 2019, due to higher cash balances and rising interest rates during most of fiscal 2020. The loss2023. Other expense resulting from foreign currency translations in fiscal years 2021, 2020 and 2019 is primarilytransactions was the result of the changes in the value of foreign currencies relative to the U.S. dollar in countries in which we operate;operate. The increase in expense during fiscal year 2023 was due to U.S. dollar denominated intercompany loans incurred in our international subsidiaries as the dollar strengthened against mostresult of these currenciesthe 3M FSD transaction on September 1, 2022. Due to our acquisition of Corvium, Inc. in all three years.
In fiscal 2021,February 2023, we received proceeds of $309,000 for a property loss settlement and recorded $300,000 of expense resulting from a legal settlement with a vendor. Additionally, adjustments to contingent consideration accruals resulted in $148,000 of income. In fiscal 2020, we took a charge to expense and recorded a reserveloss of $600,000 to provide for potential fines or penalties resulting from an administrative subpoena issued by the U.S. Treasury Department’s Office$1.5 million in fiscal year 2023 on dissolution of Foreign Asset Control. This was partially offset byour minority interest in that company. Finally, we recorded a $483,000 gain resulting from a settlement with the Brazilian governmentloss on investment during fiscal year 2023 related to sales taxes charged over several years, and proceeds received forour investment interest of a property loss settlement. In fiscal 2019, gains were recognized on insurance proceeds received for property loss settlements; additionally, adjustments were made to Quat-Chem and Deoxi contingent consideration amounts based on the level of achievement of revenue targets for the acquired businesses instart-up entity that fiscal year.
was encountering liquidity issues.

PROVISION FOR INCOME TAXES

(dollars in thousands)
  
2021
   
Change
  
2020
   
Change
  
2019
 
Provision for Income Taxes
  $14,386   12%  $12,830   0%  $12,783 

Income tax expense forduring fiscal 2021year 2023 was $14,386$0.8 million, compared to $11.9 million in the prior fiscal year, primarily resulting from the additional pre-tax loss due to the 3M FSD acquisition, share-based compensation, and foreign rate differential. This was offset primarily by an increase in GILTI income and nondeductible transaction costs.

The total amounts of unrecognized tax benefits that, if recognized, would affect the effective tax rate as of 19.1%, compared to incomeMay 31, 2023 and May 31, 2022 are $1.1 million and $0.8 million, respectively. The increase in unrecognized tax expense of $12.8 million in 2020, an effective tax rate of 17.7%. For fiscal 2019, income tax expense of $12.8 million represented an effective tax rate of 17.5%.

Differences frombenefits is primarily associated with the U. S. statutory rate of 21% to our effective rate are primarily due to provisions in the U.S. Tax Actcombined 3M FSD, including positions for transfer pricing and the exercise of stock options. Please refer to Note 6 to the consolidated financial statements for more information.
34

Table of Contents
research and development credits.

NET INCOME AND INCOME PER SHARE

Net loss was $22.9 million during fiscal year 2023, compared to net income of $48.3 million in the prior fiscal year. The decrease in earnings was primarily the result of $56.0 million of interest expense from the $1 billion in debt incurred in the Transaction, $59.8 million of transaction fees and integration expenses, and $60.9 million in incremental amortization expenses related to 3M FSD intangibles.

39


NON-GAAP FINANCIAL MEASURES

This report includes certain financial information of Neogen that differs from what is reported in accordance with GAAP. These non-GAAP financial measures consist of EBITDA, Adjusted EBITDA, Adjusted EBITDA margin, adjusted net income and adjusted earnings per share. These non-GAAP financial measures are included in this report because management believes that they provide investors with additional useful information to measure the performance of Neogen, and because these non-GAAP financial measures are frequently used by securities analysts, investors and other interested parties as common performance measures to compare results or estimate valuations across companies in Neogen’s industries.

EBITDA

We define EBITDA as net income before interest, income taxes, and depreciation and amortization. We present EBITDA as a performance measure because it may allow for a comparison of results across periods and results across companies in the industries in which Neogen operates on a consistent basis, by removing the effects on operating performance of (a) capital structure (such as the varying levels of interest expense and interest income), (b) asset base and capital investment cycle (such as depreciation and amortization) and (c) items largely outside the control of management (such as income taxes). EBITDA also forms the basis for the measurement of Adjusted EBITDA (discussed below).

Adjusted EBITDA

We define Adjusted EBITDA as EBITDA, adjusted for share-based compensation and certain transaction fees and expenses. We present Adjusted EBITDA because it provides an understanding of underlying business performance by excluding the following:

Share-based compensation. We believe it is useful to exclude share-based compensation to better understand the long-term performance of our core business and to facilitate comparison with the results of peer companies.
FX translation gain/(loss) on loan revaluation. We exclude the revaluation impacts of foreign currency fluctuations on our intercompany loan balances.
(dollars in thousands, except per share data)
  
2021
   
Change
   
2020
   
Change
   
2019
 
Net Income Attributable to Neogen
  $60,882    2%   $59,475    (1%)   $60,176 
Net Income Per Share-Basic
  $0.57     $0.57     $0.58 
Net Income Per Share-Diluted
  $0.57     $0.56     $0.57 
Certain transaction fees and expenses. We exclude fees and expenses related to certain transactions because they are outside of Neogen’s underlying core performance. These fees and expenses include deal related professional and legal fees and foreign currency transactions.
Impairment and scrap of discontinued product lines. We exclude expenses associated with impairments and inventory scrap amounts related to certain discontinued product lines.
Other one-time adjustments. We exclude one-time adjustments recorded within operating or other (expense) income to better understand the long-term performance of our core business.

Adjusted EBITDA margin

We define Adjusted EBITDA margin as Adjusted EBITDA as a percentage of total revenues. We present Adjusted EBITDA margin as a performance measure to analyze the level of Adjusted EBITDA generated from total revenue.

Adjusted Net Income

We define Adjusted Net Income as Net Income, adjusted for share-based compensation, FX translation gain/(loss) on loan revaluation, certain transaction fees and expenses, impairment and scrap of discontinued product lines and other one-time adjustments, all of which are tax effected.

Adjusted Earnings per Share

We define Adjusted Earnings per Share as Adjusted Net Income divided by diluted average shares outstanding.

40


These non-GAAP financial measures are presented for informational purposes only. EBITDA, Adjusted EBITDA, Adjusted EBITDA margin, Adjusted Net Income and Adjusted Earnings per Share are not recognized terms under GAAP and should not be considered in isolation or as a substitute for, or superior to, net income (loss), operating income, cash flow from operating activities or other measures of financial performance. This information does not purport to represent the results Neogen would have achieved had any of the transactions for which an adjustment is made occurred at the beginning of the periods presented or as of the dates indicated. This information is inherently subject to risks and uncertainties. It may not give an accurate or complete picture of Neogen’s financial condition or results of operations for the periods presented and should not be relied upon when making an investment decision.

The use of the terms EBITDA, Adjusted EBITDA, Adjusted EBITDA margin, Adjusted Net Income and Adjusted Earnings per Share may not be comparable to similarly titled measures used by other companies or persons due to potential differences in the method of calculation.

These non-GAAP financial measures have limitations as analytical tools. For example, for EBITDA-based metrics:

they do not reflect changes in, or cash requirements for, Neogen’s working capital needs;
they do not reflect Neogen’s tax expense or the cash requirements to pay taxes;
they do not reflect the historical cash expenditures or future requirements for capital expenditures or contractual commitments;
they do not reflect any cash requirements for future replacements of assets that are being depreciated and amortized; and
they may be calculated differently from other companies in Neogen’s industries limiting their usefulness as comparative measures.

A reader should compensate for these limitations by relying primarily on the financial statements of Neogen and using these non-GAAP financial measures only as a supplement to evaluate Neogen’s performance.

For each of these non-GAAP financial measures below, we are providing a reconciliation of the differences between the non-GAAP measure and the most directly comparable GAAP measure.

Reconciliation between net income and EBITDA and Adjusted EBITDA is as follows:

 

Year ended May 31

 

(in thousands)

 

2023

 

 

2022

 

 

2021

 

Net (Loss) Income

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Net income margin %

 

 

(2.8

)%

 

 

9.2

%

 

 

13.0

%

Provision for income taxes

 

 

828

 

 

 

11,900

 

 

 

14,386

 

Depreciation and amortization

 

 

88,377

 

 

 

23,694

 

 

 

21,041

 

Interest expense (income), net

 

 

52,795

 

 

 

(1,267

)

 

 

(1,614

)

EBITDA

 

$

119,130

 

 

$

82,634

 

 

$

94,695

 

Share-based compensation

 

 

10,177

 

 

 

7,154

 

 

 

6,437

 

FX transaction loss (gain) on loan revaluation(1)

 

 

5,226

 

 

 

 

 

 

 

Certain transaction fees and integration costs

 

 

59,812

 

 

 

25,581

 

 

 

3,085

 

Contingent consideration adjustments

 

 

(300

)

 

 

 

 

 

 

Restructuring

 

 

475

 

 

 

 

 

 

 

Loss on sale of minority interest

 

 

1,516

 

 

 

 

 

 

 

Loss on investment

 

 

500

 

 

 

 

 

 

 

Impairment and scrap of discontinued product lines(2)

 

 

5,639

 

 

 

 

 

 

 

Inventory step-up charge

 

 

3,245

 

 

 

 

 

 

 

Adjusted EBITDA

 

$

205,420

 

 

$

115,369

 

 

$

104,217

 

Adjusted EBITDA margin %

 

 

25.0

%

 

 

21.9

%

 

 

22.2

%

(1) Net foreign currency transaction loss (gain) associated with the revaluation of non-functional currency intercompany loans established in connection with FSD transaction.

41


(2)Expenses associated with intangible asset impairments and inventory scrap amounts related to certain discontinued product lines.

Adjusted EBITDA increased 2%$90.1 million in fiscal 2021year 2023 compared to fiscal 2020,year 2022, primarily due to earnings generated from the $6.7 million increase3M FSD business, which combined with Neogen on September 1, 2022. Expressed as a percentage of revenue, adjusted EBITDA was 25.0% in operating income. The increasefiscal year 2023 compared to 21.9% in operating incomefiscal year 2022. Increases in the margin reflect the higher margin products sold by the 3M FSD business, which was partially offset by lower othernot a part of the Company in the prior fiscal year.

Reconciliation between net income and higherAdjusted Net Income and earnings per share and Adjusted Earnings per Share are as follows:

 

Year ended May 31

 

(in thousands, except earnings per share)

 

2023

 

 

2022

 

 

2021

 

Net Income (Loss)

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Earnings per diluted share

 

$

(0.12

)

 

$

0.45

 

 

$

0.57

 

Amortization of acquisition-related intangibles

 

 

68,690

 

 

 

7,235

 

 

 

6,271

 

Share-based compensation

 

 

10,177

 

 

 

7,154

 

 

 

6,437

 

FX transaction loss (gain) on loan revaluation(1)

 

 

5,226

 

 

 

 

 

 

 

Certain transaction fees and integration costs

 

 

59,812

 

 

 

25,581

 

 

 

3,085

 

Contingent consideration adjustments

 

 

(300

)

 

 

 

 

 

 

Restructuring

 

 

475

 

 

 

 

 

 

 

Loss on sale of minority interest

 

 

1,516

 

 

 

 

 

 

 

Loss on investment

 

 

500

 

 

 

 

 

 

 

Impairment and scrap of discontinued product lines(2)

 

 

5,639

 

 

 

 

 

 

 

Inventory step-up charge

 

 

3,245

 

 

 

 

 

 

 

Other adjustments(3)

 

 

5,864

 

 

 

 

 

 

 

Estimated tax effect of above adjustments(4)

 

 

(32,323

)

 

 

(9,017

)

 

 

(1,904

)

Adjusted Net Income

 

$

105,651

 

 

$

79,260

 

 

$

74,771

 

Adjusted Earnings per Share

 

$

0.56

 

 

$

0.73

 

 

$

0.70

 

(1) Net foreign currency transaction loss (gain) associated with the revaluation of non-functional currency intercompany loans established in connection with the 3M FSD transaction.

(2) Expenses associated with intangible asset impairments and inventory scrap amounts related to certain discontinued product lines.

(3) Income tax benefit associated with non-deductible transaction costs that were recognized as expense in prior periods.

(4) Tax effect of adjustments is calculated using projected effective tax rates for each applicable item.

Adjusted Net Income increased $26.4 million during the year.

Net income decreased $701,000 in fiscal 2020 compared to fiscal 2019, primarilytwelve months ended May 31, 2023 due to the $654,000 decrease in
pre-tax
income.
higher Adjusted EBITDA.

42


FUTURE OPERATING RESULTS

Neogen Corporation’s future operating results involve a number of risks and uncertainties. Actual events or results may differ materially from those discussed in this report. Factors that could cause or contribute to such differences include, but are not limited to, the factors discussed below as well as those discussed elsewhere in this report. Management’s ability to grow the business in the future depends upon our ability to successfully implement various strategies, including:

developing, manufacturing and marketing new products with new features and capabilities, and having those new products successfully accepted in the marketplace;
expanding our markets by fostering increased use of our products by customers;
maintaining or increasing gross and net operating margins in changing cost environments;
strengthening operations and sales and marketing activities in geographies outside of the U.S.;
developing and implementing new technology development strategies; and
identifying and completing acquisitions that enhance existing product categories or create new products or services.services, and successfully integrating completed acquisitions, including the FSD transaction.

FINANCIAL CONDITION AND LIQUIDITY

On

As of May 31, 2021, we had $75.6 million in2023, the overall cash, and cash equivalents $305.5 million inand marketable securities and net working capitalposition of $537.9Neogen was $245.6 million. ForDuring the fiscal year ended May 31, 2021,2023, cash generated from operating activities was $81.2$41.0 million, compared to $85.9$68.0 million generated in fiscal 2020;2022. The decrease was primarily the result of 3M FSD transaction costs and the addition of FSD accounts receivable. Cash flow from investing activities was $201.0 million during the fiscal year ended 2023, which was primarily the result of proceeds from stock option exercises provided an additional $34.6 millionthe sale of cash. For the same period, additions tomarketable securities of $266.8 million. This was partially offset by purchases of property, equipment and other

non-current
intangible assets were $26.7of $65.8 million. Cash flow for financing activities was $118.1 million and business acquisitions used cashduring the fiscal year ended 2023, which was primarily the result of $52.0 million. We have a financing agreement with a bank providing for an unsecured revolving linethe Company paying down $100 million of credit of $15.0 million, which expiresthe $1 billion in debt taken on November 30, 2023. There were no advances against this line of credit during fiscal years 2021, 2020 and 2019, and no balance outstanding at May 31, 2021 and 2020.
to enact the FSD transaction.

Net accounts receivable atbalances were $153.3 million as of May 31, 2021 were $91.8 million,2023 compared to $84.7$99.7 million atas of May 31, 2020; the increase is primarily due to the increased sales in the fourth quarter of fiscal 2021 compared to the corresponding period a year ago. Our days2022. Days’ sales outstanding, a measurement of the time it takes to collect receivables, improved to 66for the legacy business was 57 days atas of May 31, 20212023, compared to 6862 days atas of May 31, 2020. We have been carefully monitoring2022. The increase in receivables is primarily attributable to the recording of FSD customer balances, currently managed by 3M as a transition service.

As part of transition services agreements between the Company and 3M, related to the merger of the Food Safety business, 3M is invoicing our customers for products that 3M is manufacturing and shipping on our behalf. As of May 31, 2023, there were $57.3 million in customer receivables billed by 3M on our behalf. The Company is working collaboratively with 3M on managing the credit risk associated with the former FSD customers during the period while 3M is providing transition invoicing and distribution services to the Company.

Net inventory was $133.8 million as the

COVID-19
pandemic has spread across our global markets; to date, although there has been some slowdown in collections, we have not experienced an appreciable increase in bad debt write offs.
Inventory balances were $100.7 million atof May 31, 2021,2023, an increase of $5.6$11.5 million, or 6%, compared to $95.1$122.3 million atas of May 31, 2020; excluding2022. The higher inventory fromlevels are primarily the Megazyme acquisition in December 2020,result of ongoing inflationary pressures on raw materials at our inventory is flat comparedlegacy businesses and raw material inventories purchased to a year ago. Whilesupport the FSD. Supply chain issues have moderated throughout fiscal 2023, and we took proactive measures over the last 18 monthscontinue to monitor our key raw materials to ensure adequate supplystock on hand.

Debt and Liquidity

On September 1, 2022, Neogen, 3M, and Neogen Food Safety Corporation, a subsidiary of inventory during3M created to carve out 3M’s Food Safety business, closed on the

COVID-19
pandemic, we have also continued Transaction that previously was announced in December 2021, combining 3M’s Food Safety business with Neogen in a Reverse Morris Trust transaction.

43


On June 30, 2022, Neogen Food Safety Corporation entered into a credit agreement consisting of a five-year senior secured term loan facility in the amount of $650 million and a five-year senior secured revolving facility in the amount of $150 million (collectively, the “Credit Facilities”), which became available in connection with the merger and related transactions. The loan facility was funded to focusNeogen Food Safety Corporation on improving inventory turns acrossAugust 31, 2022, and upon the business.

Neogen has been consistently profitable and has generated strong cash flow from operations during eacheffectiveness of the past three fiscal years. However,merger on September 1, 2022, became Neogen’s obligation. Financial covenants include maintaining specified levels of funded debt to EBITDA and debt service coverage. Pricing for the term loan is term SOFR plus 235 basis points. The Credit Facilities, together with the Notes described below, represent the financing incurred in connection with the merger of the 3M FSD with Neogen. In September 2022, we paid down $60 million in principal on the term loan and paid an additional $40 million in principal on the term loan in December 2022, in order to decrease the outstanding debt balance.

On July 20, 2022, Neogen Food Safety Corporation closed on an offering of $350 million aggregate principal amount of 8.625% senior notes due 2030 (the “Notes”) in a private placement at par. The Notes were initially issued by Neogen Food Safety Corporation to 3M and were transferred and delivered by 3M to the selling securityholder in the offering, in satisfaction of certain of 3M’s existing debt. Neogen Food Safety Corporation did not receive any proceeds from the sale of the Notes by the selling securityholder. Prior to the distribution of the shares of Neogen Food Safety Corporation’s common stock to 3M stockholders, the Notes were guaranteed on a senior unsecured basis by 3M. Upon consummation of such distribution, 3M was released from all obligations under its guarantee. Upon the effectiveness of the merger on September 1, 2022, the Notes became guaranteed on a senior unsecured basis by Neogen and certain wholly-owned domestic subsidiaries of Neogen.

In addition to the 3M transaction described above, our future cash on handgeneration and current borrowing capacity may not be sufficient to meet our cash requirements to fund the operating business, repay debt obligations, construct new manufacturing facilities, commercialize products currently under development or execute our future plans to acquire additional businesses, technology and products that fit within our strategic plan. Accordingly, we may be required, or may choose, to issue additional equity securities or enter into other financing arrangements for a portion of our future capital needs.

There is no guarantee that we will be successful in issuing additional equity securities or entering into other financing arrangements.

We are subject to certain legal and other proceedings in the normal course of business that have not had, and, in the opinion of management, are not expected to have, a material effect on our results of operations or financial position.

35

Table of Contents
CONTRACTUAL OBLIGATIONS

Contractual Obligations As of May 31, 2021,2023, we have the following contractual obligations due by period:

 

 

 

 

Less than

 

 

 

 

 

 

 

 

More than

 

(dollars in thousands)

 

Total

 

 

1 year

 

 

1-3 years

 

 

4-5 years

 

 

5 years

 

Long-Term Debt

 

$

900,000

 

 

$

 

 

$

 

 

$

550,000

 

 

$

350,000

 

Interest obligations

 

 

351,649

 

 

 

69,162

 

 

 

125,956

 

 

 

92,047

 

 

 

64,484

 

Operating Leases

 

 

13,895

 

 

 

3,542

 

 

 

5,739

 

 

 

2,729

 

 

 

1,885

 

Purchase Obligations (1)

 

 

100,148

 

 

 

95,620

 

 

 

4,411

 

 

 

117

 

 

 

 

 

$

1,365,692

 

 

$

168,324

 

 

$

136,106

 

 

$

644,893

 

 

$

416,369

 

(1)
Purchase obligations are primarily purchase orders for future inventory and capital equipment purchases.
       
Less than
           
More than
 
(dollars in thousands)
  
Total
   
1 year
   
1-3 years
   
3-5 years
   
5 years
 
Long-Term Debt
  $—     $—     $—     $—     $—   
Operating Leases
   2,574    1,313    1,219    42    —   
Unconditional Purchase Obligations (1)
   84,265    83,773    488    4    —   
  
 
 
   
 
 
   
 
 
   
 
 
   
 
 
 
  $86,839   $85,086   $ 1,707   $46   $ —   
(1)
Unconditional purchase obligations are primarily purchase orders for future inventory and capital equipment purchases.

We continue to make investments in our business and operating facilities. Our preliminary estimate for capital expenditures related to our legacy operations in fiscal 2024 is $30 to $40 million. We also expect to spend approximately $120 million over the next two fiscal years to construct a manufacturing facility in Lansing, Michigan to produce a significant portion of the acquired FSD products and to add additional production capacity for projected growth of existing product lines. Additionally, we expect to spend approximately $30 million over the next two fiscal years to implement a new enterprise resource planning solution.

NEW ACCOUNTING PRONOUNCEMENTS

See discussion of any New Accounting Pronouncements in Note 1 to consolidated financial statements.

36

44


ITEM 7A.
QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKS

ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKS

We have interest rate and foreign exchange rate risk exposure but no long-term fixed rate investments or borrowings.investments. Our primary interest rate risk is due to potential fluctuations of interest rates for short-term investments.

our variable rate borrowings.

Foreign exchange risk exposure arises because we market and sell our products throughout the world. Revenues in certain foreign countries as well as certain expenses related to those revenues are transacted in currencies other than the U.S. dollar. OurAs such, our operating results are exposed to changes in exchange rates between the U.S. dollar and the British pound sterling, the euro, the Mexican peso, the Brazilian real, the Chinese yuan, the Australian dollar and to a lesser extent, the Indian rupee, the Canadian dollar, the Argentine peso, the Uruguayan peso and the Chilean peso; there is also exposure to a change in exchange rate between the British pound sterling and the euro.rates. When the U.S. dollar weakens against foreign currencies, the dollar value of revenues denominated in foreign currencies increases. When the U.S. dollar strengthens, the opposite situation occurs. Additionally, previously invoiced amounts can be positively or negatively affected by changes in exchange rates in the course of collection. We use derivative financial instruments to help manage the economic impact of fluctuations in certain currency exchange rates. These contracts are adjusted to fair value through earnings.

Neogen has assets, liabilities, and operations outside of the U.S., located in Scotland, England, Ireland, Italy, Brazil, Mexico, Argentina, Uruguay, Chile, China, India, Canada and Australia where the functional currency is the British pound sterling, Brazilian real, Mexican peso, Argentine peso, Uruguayan peso, Chilean peso, Chinese yuan, Indian rupee, Canadian dollar and Australian dollar, respectively, and also transacts business throughout Europe in the euro. Our investments in foreign subsidiaries are considered to be long-term. As discussed in ITEM 1A. RISK FACTORS, our financial condition and results of operations could be adversely affected by currency fluctuations.

The following table sets forth the potential loss in future earnings or fair values, resulting from hypothetical changes in relevant market rates or prices:

Risk Category
  
Hypothetical Change
  
May 31, 2021
   
Impact
(in thousands)
      
Foreign Currency—Revenue
  10% Decrease in exchange rates  $(18,317  Earnings
Foreign Currency—Hedges
  10% Decrease in exchange rates   (1,998  Earnings
ITEM 8.
FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

Risk Category

 

Hypothetical Change

 

May 31, 2023

 

 

Impact

(dollars in thousands)

 

 

 

 

 

 

 

Foreign Currency — Revenue

 

10% Decrease in exchange rates

 

$

39,844

 

 

Earnings

Foreign Currency — Hedges

 

10% Decrease in exchange rates

 

 

1,550

 

 

Fair Value

Interest Income

 

10% Decrease in interest rates

 

 

434

 

 

Earnings

Interest Expense

 

10% Increase in interest rates

 

 

2,125

 

 

Earnings

ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

The response to this item is submitted in a separate section of this report starting on page

F-1.
ITEM 9.
CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE—NONE
ITEM 9A.
CONTROLS AND PROCEDURES

ITEM 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE—NONE

ITEM 9A. CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

An evaluation was performed under the supervision and with the participation of our management, including the Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures (as defined in Rule

13a-15
(e) under the Securities Exchange Act of 1934) as of May 31, 2021. Based on and as of the time of such evaluation, our management, including the Chief Executive Officer and Chief Financial Officer, concluded that our disclosure2023. Disclosure controls and procedures were effective as of the end of the period covered by this reportrefer to controls and other procedures designed to ensure that information required to be disclosed in the reports that are filedwe file or submittedsubmit under the Securities and Exchange Act of 1934 (the “Exchange Act”) is appropriately recorded, processed, summarized and reported, within the time periods specified in the rules and forms of the Securities and Exchange Commission’s rules and forms.Commission. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure the information required to be disclosed in the reports that are filed or submitted under the Securities Exchange Act of 1934 is accumulated and communicated to management, including the Chief Executive Officer and Chief Financial Officer, as appropriate to allow timely decisions regarding required disclosure.
37

our disclosure controls and procedures, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures werenot effective as of May 31, 2023, because of the material weaknesses described below.

45


Management’s Report on Internal Control over Financial Reporting

Management is responsible for establishing and maintaining adequate internal control over financial reporting, as such term is defined in Exchange Act Rules

13-a-15(f)
and
15d-15(f).
Our internal control over financial reporting is designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with U.S. GAAP and includes those policies and procedures that: (1) pertain to the maintenance of records that in reasonable detail accurately and fairly reflect our transactions and the dispositions of our assets; (2) provide reasonable assurance that our transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles and that our receipts and expenditures are being made only in accordance with appropriate authorizations; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of our assets that could have a material effect on our consolidated financial statements.

Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Projections of any evaluation of effectiveness for future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

On September 1, 2022, we completed our merger with Neogen Food Safety Corporation, a wholly owned subsidiary of 3M that was created to carve out 3M’s Food Safety Division. We are in the process of evaluating the existing controls and procedures of 3M's Food Safety Division and integrating it into our internal control over financial reporting. In accordance with SEC Staff guidance permitting a company to exclude an acquired business from management’s assessment of the effectiveness of internal control over financial reporting for the year in which the acquisition is completed, management has excluded the business that we acquired from our assessment of the effectiveness of internal control over financial reporting as of May 31, 2023. The business that we acquired in 3M's Food Safety Division represented approximately 82% of the Company’s total assets as of May 31, 2023, 34% of the Company’s revenues and 29% of the Company’s operating income for the year ended May 31, 2023.

Under the supervision of and with the participation of our management, including the Chief Executive Officer and Chief Financial Officer, an evaluation was conducted as towe assessed the effectiveness of our internal control over financial reporting as of May 31, 2021, based on2023, using the framework in Internal Control – Integrated Framework (2013) issuedcriteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) in Internal Control—Integrated Framework (2013). BasedA material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting, such that there is a reasonable possibility that a material misstatement of our annual or interim financial statements will not be prevented or detected on a timely basis.

Management’s assessment of the Company’s internal control over financial reporting identified the following material weaknesses that evaluation,existed as of May 31, 2023:

We identified a material weakness in internal control related to ineffective information technology general controls (ITGCs) in the areas of user access and change management over certain information technology (IT) systems that support the Company’s financial reporting processes. Specifically, we did not design and maintain: (i) sufficient logical access controls to ensure appropriate segregation of duties and adequately restrict user and privileged access to financial applications, programs and data to appropriate Company personnel; (ii) program change management controls to ensure that information technology program and data changes affecting financial information technology applications and underlying accounting records are identified, tested, authorized and implemented appropriately. As a result, manual business process controls that are dependent on the affected ITGCs were also deemed ineffective, because they could have been adversely impacted to the extent that they rely upon information and configurations from the affected IT systems.
We identified a material weakness in internal control related to ineffective period-end invoice accrual controls that are designed to ensure the completeness and accuracy of accrued expenses and accrued capital assets.

46


We identified a material weakness in internal control related to ineffective operation of management review controls related to the accounting, valuation and purchase price allocation of the Company’s acquisitions and associated goodwill. Specifically, we did not maintain adequate documentation supporting the precision of the operating effectiveness of certain associated management review controls.

These control deficiencies create a reasonable possibility that a material misstatement to the consolidated financial statements will not be prevented or detected on a timely basis, and therefore, we concluded that the deficiencies represent material weaknesses. As a result of these material weaknesses, management has concluded that our internal control over financial reporting was not effective as of May 31, 2021. 2023.

Following identification of these material weaknesses and prior to filing this Annual Report on Form 10-K, we completed additional procedures and concluded that our consolidated financial statements included in this Form 10-K have been prepared in accordance with U.S. GAAP and fairly present, in all material respects, the financial condition, results of operations and cash flows of the Company as of, and for, the periods presented in this Form 10-K.

The Company’s independent registered public accounting firm, BDO USA, P.A., which has audited and reported on our consolidated financial statements, issued an attestation report on the effectiveness of the Company’s internal control over financial reporting as of May 31, 2021 has been audited by BDO USA, LLP, an independent registered public accounting firm, as stated in its attestation report,2023, which is included onin this annual report below.

Plan of Remediation

Management has been implementing and continues to implement measures designed to ensure that control deficiencies contributing to the following pagematerial weaknesses are remediated, such that these controls are designed, implemented, and is incorporated into this Item 9A by reference.

operating effectively. The Company continues to provide additional training to personnel and put in place additional quality control measures around its processes and the retention and documentation of evidence of control activities.

When fully implemented and operational, we believe that these actions will remediate the underlying causes of the material weaknesses and strengthen our internal control over financial reporting. The material weaknesses will not be considered remediated, however, until the applicable controls operate for a sufficient period of time and management has concluded, through testing, that these controls are operating effectively.

As we implement these remediation efforts, we may determine that additional steps may be necessary to remediate the material weaknesses. We cannot provide assurance that these remediation efforts will be successful or that our internal control over financial reporting will be effective in accomplishing all control objectives all of the time. We will continue to assess the effectiveness of our remediation efforts in connection with our evaluations of internal control over financial reporting.

Changes in Internal Control over Financial Reporting

No

Other than the material weaknesses and related remediation efforts described above, and any changes resulting from the business combination described above, no changes in our internal control over financial reporting were identified as having occurred during the quarter ended May 31, 20212023 that have materially affected, or are reasonably likely to materially affect, internal control over financial reporting.

ITEM 9B.
OTHER INFORMATION—NONE
ITEM 9C.
DISCLOSURE REGARDING FOREIGN JURISDICTIONS THAT PREVENT INSPECTIONS—NOT APPLICABLE
38

47


Report of Independent Registered Public Accounting Firm

Shareholders and Board of Directors

Neogen Corporation

Grand Rapids,

Lansing, Michigan

Opinion on Internal Control over Financial Reporting

We have audited Neogen Corporation’s (the “Company’s”) internal control over financial reporting as of May 31, 2021,2023, based on criteria established in

Internal Control Integrated Framework (2013)
issued by the Committee of Sponsoring Organizations of the Treadway Commission (the “COSO criteria”). In our opinion, the Company maintained,did not maintain, in all material respects, effective internal control over financial reporting as of May 31, 2021,2023, based on the COSO criteria
.
criteria. We do not express an opinion or any other form of assurance on management’s statements referring to any corrective actions taken by the Company after the date of management’s assessment.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States) (“PCAOB”), the consolidated balance sheets of the Company as of May 31, 20212023 and 2020,2022, the related consolidated statements of income (loss), comprehensive income, stockholders’ equity, and cash flows for each of the three years in the period ended May 31, 2021,2023, and the related notes and our report dated July 30, 2021August 15, 2023 expressed an unqualified opinion thereon.

Basis for Opinion

The Company’s management is responsible for maintaining effective internal control over financial reporting and for its assessment of the effectiveness of internal control over financial reporting, included in the accompanying Item 9A, Management’s Report on Internal Control over Financial Reporting. Our responsibility is to express an opinion on the Company’s internal control over financial reporting based on our audit. We are a public accounting firm registered with the PCAOB and are required to be independent with respect to the Company in accordance with U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audit of internal control over financial reporting in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, and testing and evaluating the design and operating effectiveness of internal control based on the assessed risk. Our audit also included performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.

A material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting, such that there is a reasonable possibility that a material misstatement of the Company’s annual or interim financial statements will not be prevented or detected on a timely basis. Material weaknesses have been identified and described in management’s assessment. These material weaknesses related to management’s failure to design and maintain effective controls over financial reporting, specifically related to the following: (1) information technology general controls in the areas of user access and change management over certain information technology systems that support the Company’s financial reporting processes, (2) period-end invoice accrual controls and (3) management review controls related to the accounting, valuation and purchase price allocation of the Company’s acquisitions and associated goodwill. These material weaknesses were considered in determining the nature, timing, and extent of audit tests applied in our audit of the 2023 consolidated financial statements, and this report does not affect our report dated August 15, 2023 on those consolidated financial statements.

As indicated in the accompanying “Item 9A, Changes in Internal Control over Financial Reporting”, management’s assessment of and conclusion on the effectiveness of internal control over financial reporting did not include the internal controls of 3M’s Food Safety Division, which was acquired on September 1, 2022, and which is included in the consolidated balance sheet of the Company as of May 31, 2023, and the related consolidated statements of income (loss), comprehensive income, stockholders’ equity, and cash flows for the year then ended. 3M’s Food Safety Division constituted 82% of total assets as of May 31, 2023, and 34% and 29% of revenues and operating

48


income, respectively, for the year then ended. Management did not assess the effectiveness of internal control over financial reporting of 3M’s Food Safety Division because of the timing of the acquisition which was completed on September 1, 2022. Our audit of internal control over financial reporting of the Company also did not include an evaluation of the internal control over financial reporting of 3M’s Food Safety Division.

Definition and Limitations of Internal Control over Financial Reporting

A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’s internal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements.

Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

/s/ BDO USA, LLP

P.A.

Grand Rapids, Michigan

July 30, 2021

39

August 15, 2023

49


ITEM 9B. OTHER INFORMATION—NONE

ITEM 9C. DISCLOSURE REGARDING FOREIGN JURISDICTIONS THAT PREVENT INSPECTIONS—NOT APPLICABLE

50


PART III

ITEM 10.
DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE

ITEM 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE

Information regarding the Company and certain corporate governance matters appearing under the captions “Proposal 1—1 — Election of Directors,” “Information About the Board and Corporate Governance Matters,” and “Miscellaneous-Delinquent“Additional Information-Delinquent Section 16(a) Reports” is incorporated by reference to Neogen’s 20212023 proxy statement to be filed within 120 days of May 31, 2021.

2023.

We have adopted a Code of Conduct that applies to our directors, officers, and employees. This Code of Conduct is available on our website at

https://www.Neogen.com/globalassets/pdfs/corporate-governance-sec-and-investor-information/codeofconduct.pdf
. We intend to satisfy the disclosure requirement regarding any amendment to, or a waiver from, a provision of the code of conduct for our principal executive officer, principal financial officer, principal accounting officer or controller, or persons performing similar functions, by posting such information on our website.

Information About Our Officers and Executive Officers

The officers of Neogen serve at the discretion of the Board of Directors. The names and titles of our officers as of May 31, 20212023 are set forth below.

Name

Position with the Company

Year Joined
the Company

John E. Adent

President & Chief Executive Officer

2017

Joseph A. Corbett
Vice President, Animal Safety Sales
1993

Robert S. Donofrio, Ph.D.

Vice President, Research & Development

Chief Scientific Officer

2016

Shane M. Fitzwater
Vice President, Animal Safety Operations
2018
Jerome L. Hagedorn
Vice President, North American Operations
2018

Douglas E. Jones

Vice President &

Chief CommercialOperating Officer

2020

Jason W. Lilly, Ph.D.

Vice President, International Business

Americas & Australia/New Zealand

2005

Julie L. Mann

Vice President &

Chief Human Resources Officer

2017

Marylinn Munson

David H. Naemura

Vice President, Agrigenomics

Chief Financial Officer

2020

2022

Steven J. Quinlan

Vice President, & Chief Financial Officer

Finance

2011

Amy M. Rocklin, Ph.D.

Vice President, General Counsel

Chief Legal & Corporate Secretary

Compliance Officer

2021

Information concerning the officers of Neogen follows:

John E. Adent, age 53,55, joined Neogen as Chief Executive Officer on July 17, 2017 and was then named President on September 22, 2017. Prior to joining Neogen, Mr. Adent served as the Chief Executive Officer of Animal Health International, Inc., formerly known as Lextron, Inc., from 2004 to 2015, also serving as its President during that time. Animal Health International was sold to Patterson Companies, Inc. in 2015, and Mr. Adent served as the Chief Executive Officer of the $3.3 billion Animal Health Division of Patterson Animal Health from that period until his resignation on July 1, 2017. Mr. Adent began his career with management responsibilities for Ralston Purina Company, developing animal feed manufacturing and sales operations in China and the Philippines. When Ralston Purina spun off that business to Agribrands, he continued his management role in the European division in Spain and Hungary, serving as managing director of the Hungarian operations. He left Ralston Purina in 2004.

Joseph A. Corbett, age 52, joined Neogen in December 1993 as a sales representative in the Animal Safety operation based in Lexington, Kentucky. Prior to joining Neogen, he worked for the Marriott Corporation in sales and operations. He has served in various sales, marketing and operational roles in the Neogen Animal Safety segment. He was named Vice President, Animal Safety Sales in October 2014, responsible for all Animal Safety revenues, excluding Genomics and Life Sciences.
40

Dr. Robert S. Donofrio, age 48,50, joined Neogen in February 2016 as Director of Microbiology Research and Development, and was promoted to Director of Food Safety Research and Development in December 2016. In April 2018, Dr. Donofrio was named Vice President, Food Safety Research and Development.Development and then named Vice President, Research and Development in September 2018. In 2022, Dr. Donofrio was named Chief Scientific Officer. Prior to joining Neogen, he worked for 15 years at NSF International in various positions of increasing responsibility, including Director of Microbiology and Molecular Biology and Director of Applied Research, where he led efforts in grant research and method development with partners in academia, industry and government. At Neogen, Dr. Donofrio is responsible for our worldwide food safety and animal safety research activities.

Shane M. Fitzwater, age 48, joined Neogen in April 2018 as Vice President, Animal Safety Operations. In his role, Mr. Fitzwater is responsible for manufacturing, quality systems, supply chain, shipping and warehousing for our Animal Safety operations, excluding Genomics. Prior to joining Neogen, he spent 18 years in positions of increasing responsibility at Ecolab, Inc., including five years as Ecolab’s Vice President of Supply Chain, Global Specialty Sector. Mr. Fitzwater managed Ecolab’s global supply chain for a $750 million business unit with worldwide manufacturing and logistics operations. Before being named a vice president, he spent four years as a director of operations at Ecolab, managing a group of 450 employees and an annual operating budget of $40 million.
Jerome L. Hagedorn, age 55, joined Neogen in April 2018 as Vice President, Food Safety Operations; in 2020, he was named Vice President, North American Operations. In the role, Mr. Hagedorn is responsible for the manufacturing, supply chain, shipping and warehousing, production engineering and quality systems for Neogen’s North American operations. Prior to joining Neogen, Mr. Hagedorn spent the past eight years as Vice President of Operations at Siemens Healthcare Diagnostics. At Siemens, he was responsible for multiple plant operations, including diagnostic instrument manufacturing and new product introduction. Prior to joining Siemens, Mr. Hagedorn held a variety of senior level positions over a 20 year career, including Director of Manufacturing at Bayer Healthcare in Indiana, Director of Lean Manufacturing at Invensys in Ohio, and Manager of Automated Manufacturing at Siemens Electronic Components in Mexico.

51


Douglas E. Jones, age 51,53, joined Neogen as Chief Commercial Officer on August 17, 2020.2020; in 2022, he was named Chief Operating Officer. Prior to joining Neogen, Mr. Jones served as the President of the Companion Animal Division at Patterson Companies from 2016 to August 2020. Prior to joining Patterson, Mr. Jones served as the Head of Business Operations for the North American Merial Animal Health Division of Sanofi. Mr. Jones began his career as a management consultant with the North Highland Company and PriceWaterhouseCoopers, focusing on commercial transformation and strategy projects in the pharmaceutical, healthcare distribution and high-tech industries.

Dr. Jason W. Lilly, age 47,49, joined Neogen in June 2005 as Market Development Manager for Food Safety. In June 2009, he moved to the Corporate Development group. He was named Vice President of Corporate Development in December 2011, responsible for the identification and acquisition of new business opportunities for the Company. In January 2019, Dr. Lilly was named Vice President, International Business, responsible for Neogen’s operations outside of the U.S. and Canada. In May 2023, Dr. Lilly was named Vice President, Americas & Australia/New Zealand, with responsibility for all commercial business in those regions. He also has strategic and operational oversight of our global genomics business. Prior to joining Neogen, he served in various technical sales and marketing roles at Invitrogen Corporation.

Julie L. Mann, age 56,58, joined Neogen in 2017 as Director of Human Resources and was promoted to Senior Director of Human Resources in June 2019. On June 1,In 2020, Ms. Mann was named Vice President & Chief Human Resources Officer, with responsibilities for people-focused programs and initiatives for Neogen’s more than 1,800 globalworldwide employees. Ms. Mann has more than 30 years of experience focused on all aspects of strategic human resources including talent acquisition, compensation and benefits, employee development and employee relations. Prior to joining Neogen, Ms. Mann held the positions of Director, Talent Acquisition at Holland, a logistics company, and Director, People Services Consulting at Herman Miller.

Marylinn Munson,

David H. Naemura, age 57,54, joined Neogen in MayNovember 2022 as Chief Financial Officer. Previously, Mr. Naemura served as the Senior Vice President and Chief Financial Officer of Vontier Corporation from February 2020 until November 2022. Mr. Naemura served as Chief Financial Officer of Gates Industrial Corporation from March 2015 to January 2020. Prior to his time at Gates Industrial Corporation, Mr. Naemura served as Vice President Agrigenomics. Ms. Munson has held positions with increasing responsibilityof Finance and Group Chief Financial Officer at Danaher Corporation from April 2012 to March 2015, and previously served as Danaher Corporation’s Test & Measurement Communications Platform Chief Financial Officer from January 2009 to April 2012. Prior to 2009, Mr. Naemura was employed by Tektronix Corporation from August 2000 to January 2009, including during its acquisition by Danaher Corporation in sales and operations in the life science, biotechnology and agriculture industries for more than 20 years, with an additional seven years of experience in clinical and research labs. In the five years prior to joining Neogen, Ms. Munson was Board Chair at NorthShore Bio, Sr Partner at TNK Associates, LLC (dba Devil Doc Distributors) and provided consulting services at MPower Network. Her previous positions included VP of Global NGS Informatics at Qiagen, VP of Global Business Development and Sales at Biomatrica, Director of Global Sales Operations and America Sales at Illumina, and Global Market/Business Development Manager at Agilent Technologies.

2007.

Steven J. Quinlan, age 58,60, joined Neogen in January 2011 as Vice President & Chief Financial Officer and was also Corporate Secretary until March 2021. HeMr. Quinlan announced his retirement in September 2022 and Mr. Naemura was subsequently appointed as Chief Financial Officer, beginning in November 2022. For the remainder of fiscal year 2023, Mr. Quinlan continued to serve the Company as Vice President of Finance and is continuing to work on special projects through the end of the 2023 calendar year. Prior to his retirement announcement, Mr. Quinlan was responsible for all internal and external financial reporting for Neogen, and managesmanaged the accounting, information technology, corporate purchasing, treasury and investor relations functions. Mr. Quinlan came to Neogen following 19 years at Detrex Corporation (1992-2010), the last eight years serving as Vice President-Finance, CFO and Treasurer. He was on the audit staff at the public accounting firm Price Waterhouse (now PWC)PricewaterhouseCoopers) from 1985-1989.

Amy M. Rocklin, Ph.D., age 49,51, joined Neogen in March 2021 as Vice President, General Counsel & Corporate Secretary. In 2022, Dr. Rocklin was named Chief Legal & Compliance Officer. In this role, she is responsible for all legal and compliance matters and also leads the regulatory, quality and ESG functions. Dr. Rocklin also serves as the Corporate Secretary. Prior to joining Neogen, Dr. Rocklin was the Division Vice President, Corporate Law at Corning Incorporated, one of the world’s leading innovators in materials science.Incorporated. In her nearly ten years at

41

Corning, she held multiple leadership positions within Corning’s Law Department, including Director of Law, M&A and Emerging Innovations. Before Corning, Dr. Rocklin held leadership positions at Smiths Group plc and was in private practice at the law firm of Foley & Lardner LLP.
ITEM 11.
EXECUTIVE COMPENSATION

52


ITEM 11. EXECUTIVE COMPENSATION

The information required by this Item, and pursuant to Regulation 14A of the Exchange Act, is incorporated by reference from the sections entitled “Compensation Discussion and Analysis”, “Compensation Committee Report”, “Executive Compensation”, “Information About the Board and Corporate Governance Matters-Compensation Committee Interlocks and Insider Participation”, “CEO Pay Ratio”, and “Compensation of Directors” in the Company’s definitive Proxy Statement to be filed within 120 days of May 31, 2021.

ITEM 12.
SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT, AND RELATED STOCKHOLDER MATTERS
2023.

ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT, AND RELATED STOCKHOLDER MATTERS

The information required by this Item, and pursuant to Regulation 14A of the Exchange Act, is incorporated by reference from the section entitled “Security Ownership of Certain Beneficial Owners, Directors and Management” in the Company’s definitive Proxy Statement to be filed within 120 days of May 31, 2021.

ITEM 13.
CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE
2023.

ITEM 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE

The information required by this Item, and pursuant to Regulation 14A of the Exchange Act, is incorporated by reference from the section entitled “Information about the Board and Corporate Governance Matters-Independent Directors”Directors,” “Board Committees” and “-Certain“Certain Relationships and Related Party Transactions” in the Company’s definitive Proxy Statement to be filed within 120 days of May 31, 2021.

ITEM 14.
PRINCIPAL ACCOUNTANT FEES AND SERVICES
2023.

ITEM 14. PRINCIPAL ACCOUNTANT FEES AND SERVICES

The information required by this Item, and pursuant to Regulation 14A of the Exchange Act, is incorporated by reference from the section entitled “Proposal 3

Ratification of the Appointment of the Company’s Independent Registered Public Accounting Firm” in the Company’s definitive Proxy Statement to be filed within 120 days of May 31, 2021.
2023.

53


PART IV

ITEM 15.
EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

ITEM 15. EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

(a) (1) and (2) and (c). The response to this portion of ITEM 15 is submitted as a separate section of this report starting on page

F-1.

(a) (3) and (b). The Exhibits, listed on the accompanying Exhibit Index on page 40, are incorporated herein by reference.

ITEM 16.
FORM
10-K
SUMMARY — NONE
42

ITEM 16. FORM 10-K SUMMARY — NONE

Neogen Corporation

Annual Report on Form

10-K

Year Ended May 31, 2021

2023

EXHIBIT INDEX

EXHIBIT NO.

DESCRIPTION

  3.1

2.1

Restated ArticlesAgreement and Plan of Incorporation,Merger, dated as amended on November 23, 2011of December 13, 2021, by and among 3M Company, Neogen Food Safety Corporation, Neogen Corporation and Nova RMT Sub, Inc. (incorporated by reference to Exhibit 3.1 filed with2.1 to the Registrant’s QuarterlyCurrent Report on Form 10-Q8-K filed by Neogen Corporation on December 30, 2011)15, 2021).

  3.2

2.2

Separation and Distribution Agreement, dated as of December 13, 2021, by and among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 2.2 to the Current Report on Form 8-K filed by Neogen Corporation on December 15, 2021).

2.3

Amendment No. 1 to the Separation and Distribution Agreement, dated as of August 31, 2022, by and among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 2.2 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

2.4

Asset Purchase Agreement, dated as of December 13, 2021, by and between 3M Company and Neogen Corporation (incorporated by reference to Exhibit 2.3 to the Current Report on Form 8-K filed by Neogen Corporation on December 15, 2021).

3.1

Certificate of Amendment to Articles of Incorporation filed on October 11, 2010 (incorporated by reference to Exhibit 3.2 filed with the Registrant’s Annual Report on Form 10-K filed on July 30, 2020).

  3.3

3.2

Restated Articles of Incorporation, as amended on November 23, 2011 (incorporated by reference to Exhibit 3.1 filed with the Registrant’s Quarterly Report on Form 10-Q filed December 30, 2011).

3.3

Certificate of Amendment to Articles of Incorporation filed on November 20, 2018 (incorporated by reference to Exhibit 3 filed with the Registrant’s Quarterly Report on Form 10-Q filed December 28, 2018).

3.4

Certificate of Amendment to Articles of Incorporation of Neogen Corporation filed on March 14, 2022 (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed by Neogen Corporation on March 17, 2022).

3.5

Certificate of Amendment to Articles of Incorporation of Neogen Corporation filed on September 1, 2022 (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

3.6

By-Laws, as amended (incorporated by reference to Exhibit 3.2 to the Registrant’s Quarterly Report on Form 10-Q filed April 14, 2000).

10.1

3.7

Neogen Corporation 2007 Stock Option PlanAmendment to the By-Laws, as amended and restated (incorporated by reference to Exhibit A3.2 to the Registrant’s 2011 Proxy Statement August 31, 2011Current Report on Form 8-K filed by Neogen Corporation on September 1, 2011)2022).

4.1

Senior Notes Indenture for 8.625% Senior Notes due 2030, dated as of July 20, 2022, among Neogen Food Safety Corporation, as issuer, the guarantors party thereto from time to time, and U.S.

54


10.2

EXHIBIT NO.

DESCRIPTION

Neogen Corporation 2015 Omnibus Incentive PlanBank Trust Company, National Association, as trustee (incorporated by reference to Appendix AExhibit 10.10 to Neogen’s Registration Statement on Form S-4 (Registration No. 333-263667), filed with the Registrant’s 2015 Proxy Statement dated and filed August 25, 2015)SEC on July 27, 2022).

10.3

4.2

Supplemental Indenture, dated as of September 1, 2022, among Neogen Food Safety Corporation (f/k/a Neogen Food Safety Corporation), as issuer, U.S. Bank Trust Company, National Association, as trustee, Neogen Corporation 2018 Omnibus Incentive Planand certain of its subsidiaries (incorporated by reference to Appendix AExhibit 4.2 to the Registrant’s 2018 Proxy Statement dated andCurrent Report on Form 8-K filed August 28, 2018)by Neogen Corporation on September 1, 2022).

10.4

10.1

AmendedTax Matters Agreement, dated as of September 1, 2022, by and Restated among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.2

Intellectual Property Cross-License Agreement, dated as of September 1, 2022, by and between 3M Company and Neogen Food Safety Corporation (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.3

Trademark Transitional License Agreement, dated as of September 1, 2022, by and among 3M Company, 3M Innovative Properties Company, Neogen Corporation and Neogen Food Safety Corporation (incorporated by reference to Exhibit 10.3 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.4

Transition Services Agreement, dated as of September 1, 2022, by and among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 10.4 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.5

Transition Distribution Services Agreement, dated as of September 1, 2022, by and among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 10.5 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.6

Transition Contract Manufacturing Agreement, dated as of September 1, 2022, by and among 3M Company, Neogen Food Safety Corporation and Neogen Corporation (incorporated by reference to Exhibit 10.6 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.7

Clean-Trace(TM) Distribution Agreement, dated as of September 1, 2022, by and between 3M Company and Neogen Food Safety Corporation (incorporated by reference to Exhibit 10.7 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.8

Real Estate License Agreement, dated as of September 1, 2022, by and among certain subsidiaries of Neogen Corporation, 3M Company and certain of its subsidiaries (incorporated by reference to Exhibit 10.8 to the Current Report on Form 8-K filed by Neogen Corporation on September 1, 2022).

10.9

Credit Agreement, dated as of NovemberJune 30, 2016 between Registrant2022, among Neogen Food Safety Corporation, as borrower, the lenders from time to time party thereto, and JP MorganJPMorgan Chase Bank, N.A., as administrative agent, and joined thereto as of September 1, 2022 by Neogen Corporation, as a borrower (incorporated by reference to Exhibit 10.A of10.9 to Neogen’s Registration Statement on Form S-4 (Registration No. 333-263667), filed with the Registrant’s Form 8-K fileSEC on December 6, 2016)July 27, 2022).

10.5

21

First Amendment to Amended and Restated Credit Agreement dated as of November 30, 2018 between Registrant and JPMorgan Chase N.A. (incorporated by reference to Exhibit 10.A to the Registrant’s Form 8-K filed on December 6, 2018).

10.6Second Amendment to Amended and Restated Credit Agreement dated as of November 30, 2020 between Registrant and JP Morgan Chase N.A. (incorporated by reference to Exhibit 10.A of the Registrant’s Form 8-K filed on December 17, 2020).
21Listing of Subsidiaries

23

Consent of Independent Registered Public Accounting Firm BDO USA, LLPP.A.

24

Power of Attorney

31.1

Section 302 Certification of Principal Executive Officer

31.2

Section 302 Certification of Principal Financial Officer

32

Certification Pursuant to 18 U.S.C Section 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

101.INS

Inline XBRL Instance Document

101.SCH

Inline XBRL Taxonomy Extension Schema Document

101.CAL

Inline XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF

Inline XBRL Taxonomy Extension Definition Document

101.LAB

Inline XBRL Taxonomy Extension Label Linkbase Document

55


101.PRE

EXHIBIT NO.

DESCRIPTION

101.PRE

Inline XBRL Taxonomy Extension Presentation Linkbase Document

104

Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101)

43

56


SIGNATURES

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the Registrant has duly caused this Report to be signed on its behalf by the undersigned, thereunto duly authorized.

NEOGEN CORPORATION

By:

 By:

/s/ John E. Adent

By:

By:

/s/ Steven J. Quinlan

David H. Naemura

John E. Adent, President & Chief

Steven J. Quinlan, Vice President &

David H. Naemura,

Executive Officer

Chief Financial Officer

(Principal Executive Officer)

(Principal Financial & Accounting Officer)

Dated: July 30, 2021

August 15, 2023

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the Registrant and in the capacities and on the dates indicated.

Signature

Title

Date

Title

President & Chief Executive Officer

Date

/s/ John E. Adent

(Principal Executive Officer)

August 15, 2023

John E. Adent

Chief Financial Officer

/s/ David H. Naemura

(Principal Financial & Accounting Officer)

August 15, 2023

David H. Naemura

*

Chairman of the Board of Directors

August 15, 2023

James C. Borel

*

Director

August 15, 2023

William T. Boehm, Ph.D.

*

Director

August 15, 2023

Jeffrey D. Capello

*

Director

August 15, 2023

Ronald D. Green, Ph.D.

*

Director

August 15, 2023

Aashima Gupta

*

Director

August 15, 2023

Raphael A. Rodriguez

*

Director

August 15, 2023

James P. Tobin

*

Director

August 15, 2023

Darci L. Vetter

57


Signature

Title

Date

*

Director

August 15, 2023

Catherine E. Woteki, Ph.D.

*By:

/s/ John E. Adent

President & Chief Executive Officer (Principal Executive Officer)July 30, 2021

John E. Adent,

Attorney-in-fact

/s/ Steven J. Quinlan
Vice President & Chief Financial Officer
(Principal Financial & Accounting Officer)
July 30, 2021
Steven J. Quinlan
*
Chairman of the Board of DirectorsJuly 30, 2021
James C. Borel
*
DirectorJuly 30, 2021
William T. Boehm, Ph.D.
*
DirectorJuly 30, 2021
Ronald D. Green, Ph.D.
*
DirectorJuly 30, 2021
Ralph A. Rodriguez
*
DirectorJuly 30, 2021
James P. Tobin
*
DirectorJuly 30, 2021
Darci L. Vetter
*
DirectorJuly 30, 2021
Catherine E. Woteki, Ph.D.

August 15, 2023

*By:/s/ John E. Adent
John E. Adent,
Attorney-in-fact
July 30, 2021                        
44

58


ANNUAL REPORT ON FORM

10-K

ITEM 15 (a)(1)(a)(2) and (c)

LIST OF FINANCIAL STATEMENTS AND FINANCIAL STATEMENT SCHEDULES

YEAR ENDED MAY 31, 2021

2023

NEOGEN CORPORATION

LANSING, MICHIGAN

FORM

10-K—ITEM
15(a)(1) AND (2) AND 15(c)

LIST OF FINANCIAL STATEMENTS AND FINANCIAL STATEMENT SCHEDULES

The following consolidated financial statements of Neogen Corporation and subsidiaries are included below and incorporated in ITEM 8:

BDO USA, P.A., Grand Rapids, MI PCAOB ID# 243

F-2

Sheets

F-4

Income (Loss)

F-6

Income

F-7

Equity

F-8

Flows

F-9

Notes to Consolidated Financial Statements

F-10

Schedules for which provision is made in the applicable accounting regulation of the United States Securities and Exchange Commission are not required under the related instructions or are inapplicable and, therefore, have been omitted.

F-1


Report of Independent Registered Public Accounting Firm

Shareholders and Board of Directors

Neogen Corporation

Lansing, Michigan

Opinion on the Consolidated Financial Statements

We have audited the accompanying consolidated balance sheets of Neogen Corporation (the “Company”) as of May 31, 20212023 and 2020,2022, the related consolidated statements of income (loss), comprehensive income, stockholders’ equity, and cash flows for each of the three years in the period ended May 31, 2021,2023, and the related notes (collectively referred to as the “consolidated financial statements”). In our opinion, the consolidated financial statements present fairly, in all material respects, the financial position of the Company at May 31, 20212023 and 2020,2022, and the results of its operations and its cash flows for each of the three years in the period ended May 31, 2021

,
2023, in conformity with accounting principles generally accepted in the United States of America.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States) (“PCAOB”), the Company’s internal control over financial reporting as of May 31, 2021,2023, based on criteria established in

Internal Control – Integrated Framework (2013)
issued by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”) and our report dated July 30, 2021August 15, 2023 expressed an unqualifiedadverse opinion thereon.

Basis for Opinion

These consolidated financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on the Company’s consolidated financial statements based on our audits. We are a public accounting firm registered with the PCAOB and are required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the consolidated financial statements are free of material misstatement, whether due to error or fraud.

Our audits included performing procedures to assess the risks of material misstatement of the consolidated financial statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, evidence regarding the amounts and disclosures in the consolidated financial statements. Our audits also included evaluating the accounting principles used and significant estimates made by management, as well as evaluating the overall presentation of the consolidated financial statements. We believe that our audits provide a reasonable basis for our opinion.

F-2

Critical Audit Matter

The critical audit matter communicated below is a matter arising from the current period audit of the consolidated financial statements that was communicated or required to be communicated to the audit committee and that: (1) relates to accounts or disclosures that are material to the consolidated financial statements and (2) involved our especially challenging, subjective, or complex judgments. The communication of critical audit matters does not alter in any way our opinion on the consolidated financial statements, taken as a whole, and we are not, by communicating the critical audit matter below, providing separate opinions on the critical audit matter or on the accounts or disclosures to which it relates it relates.

Evaluation

Valuation of the Accounting for Income Taxes

customer relationships intangible asset – 3M Food Safety Division transaction

As described in Notes 1 and 6Note 3 to the consolidated financial statements, on September 1, 2022, the Company recorded income tax expensecompleted a transaction combining 3M’s Food Safety Division with Neogen in a Reverse Morris Trust transaction for consideration of approximately $3.2 billion, which resulted in recording of a customer relationships intangible asset valued at $1.17 billion. Management determined the fair value of the acquired customer relationships intangible asset by applying the multi-period excess earnings method, which involved the use of significant estimates and assumptions related to U.S.forecasted revenue growth rate and Foreign tax paying jurisdictions totaling $14.39 million for the year ended May 31, 2021. International components of U.S. income taxes have a significant impact on total income tax expense including global intangible

low-taxed
income and Subpart F income representing $2.69 million of expense and foreign derived intangible income deduction and foreign tax credits which provide income tax benefit of $3.96 million. The Company’s accounting for income taxes involves the application of tax regulations in each of the tax paying jurisdictions in which it operates. The determination of income subject to income tax in each tax paying jurisdiction requires management to apply transfer pricing guidelines for certain intercompany transactions. Additionally, the Company is entitled to claim foreign tax credits for taxes paid in international tax paying jurisdictions. Management’s assumptions and allocations used in the determination of the foreign tax credits are based on current interpretations of complex income tax regulations and can have a material effect on the calculation of U.S. income taxes.
customer attrition rate.

F-2


We identified the assumptions and allocations used to calculate international componentsvaluation of U.S. income taxes to bethe customer relationship intangible asset from the 3M Food Safety Division transaction as a critical audit matter. TheseThe principal considerations for this determination are the significant judgments and assumptions made by management when determining the fair value of the customer relationships intangible asset, specifically the forecasted revenue growth rate and allocations include: (i) technical merit of tax positions including considerations related to transfer pricing guidelines for certain intercompany transactions, and (ii) allocation methodologies that are subjective in nature.customer attrition rate. Auditing these assumptions and allocationselements involved especially subjective auditor judgment due to the complexitynature and extent of audit effort required to address these matters, including the extent of specialized skills or knowledge needed.

The primary procedures we performed to address this critical audit matter included:

AssessingUtilizing personnel with specialized knowledge and skills in valuation to assist in (i) evaluating management’s process for estimating the designfair value of the customer relationship intangible asset, and testing operating effectiveness of certain controls over(ii) evaluating the Company’s income tax provision process, including controls over the identification and application of tax laws over earnings from multiple tax jurisdictionsmethodology used and the process to assessreasonableness of the technical meritsattrition rate.
Evaluating the reliability of tax positions taken.
the underlying data provided by management.
Evaluating the reasonableness and appropriateness of the significant assumptions related to the forecasted revenue growth rate by (i) analyzing the current and past performance of the former 3M Food Safety Division, (ii) evaluating the consistency with external market and industry data, used to developand (iii) comparing the assumptions and allocations made by management against relevantconsistency with evidence obtained in other areas of the audit.
Utilizing professionals with specialized skills and knowledge in taxation to evaluate the Company’s application of the applicable tax laws, the technical merit of tax positions taken, and the reasonableness of the Company’s apportionment methodologies used.

/s/ BDO USA, LLP

P.A.

We have served as the Company’s auditor since 2014.

July 30, 2021

Grand Rapids, Michigan

August 15, 2023

F-3


Neogen Corporation and Subsidiaries

Consolidated Balance Sheets – Assets

(in thousands)

   
May 31
 
   
2021
   
2020
 
Assets
          
   
Current Assets
          
Cash and cash equivalents
  $75,602   $66,269 
Marketable securities
   305,485    277,404 
Accounts receivable, net of allowance of $1,400 and $1,350 at
May 31, 2021 and 2020, respectively
   91,823    84,681 
Inventories
   100,701    95,053 
Prepaid expenses and other current assets
   17,840    13,999 
           
Total Current Assets
   591,451    537,406 
   
Property and Equipment
          
Land and improvements
   7,783    5,456 
Building and improvements
   72,754    48,881 
Machinery and equipment
   108,194    90,351 
Furniture and fixtures
   6,270    4,324 
Construction in progress
   3,261    4,968 
           
    198,262    153,980 
Less accumulated depreciation
   (97,809)   (75,309)
           
Net Property and Equipment
   100,453    78,671 
   
Other Assets
          
Right of use assets
   2,477    1,952 
Goodwill
   131,476    110,340 
Other
non-amortizable
intangible assets
   15,545    15,217 
Amortizable intangible assets, net of accumulated amortization of $53,462 and $44,690

at May 31, 2021 and 2020, respectivel
y
   76,771    51,364 
Other
non-current
assets
   2,019    2,232 
           
Total Other Assets
   228,288    181,105 
           
Total Assets
  $ 920,192   $797,182 
           

 

May 31

 

 

2023

 

 

2022

 

Assets

 

 

 

 

 

 

Current Assets

 

 

 

 

 

 

Cash and cash equivalents

 

$

163,240

 

 

$

44,473

 

Marketable securities

 

 

82,329

 

 

 

336,578

 

Accounts receivable, net

 

 

153,253

 

 

 

99,674

 

Inventories

 

 

133,812

 

 

 

122,313

 

Prepaid expenses and other current assets

 

 

53,297

 

 

 

23,760

 

Total Current Assets

 

 

585,931

 

 

 

626,798

 

Property and Equipment

 

 

 

 

 

 

Land and improvements

 

 

10,209

 

 

 

9,485

 

Building and improvements

 

 

96,794

 

 

 

79,513

 

Machinery and equipment

 

 

152,547

 

 

 

114,180

 

Furniture and fixtures

 

 

7,080

 

 

 

6,307

 

Construction in progress

 

 

52,237

 

 

 

5,974

 

 

 

318,867

 

 

 

215,459

 

Less accumulated depreciation

 

 

(120,118

)

 

 

(104,875

)

Net Property and Equipment

 

 

198,749

 

 

 

110,584

 

Other Assets

 

 

 

 

 

 

Right of use assets

 

 

11,933

 

 

 

3,184

 

Goodwill

 

 

2,137,496

 

 

 

142,704

 

Other non-amortizable intangible assets

 

 

14,316

 

 

 

15,397

 

Amortizable intangible assets, net

 

 

1,590,787

 

 

 

92,106

 

Other non-current assets

 

 

15,220

 

 

 

2,156

 

Total Other Assets

 

 

3,769,752

 

 

 

255,547

 

Total Assets

 

$

4,554,432

 

 

$

992,929

 

See accompanying notes to consolidated financial statements.

F-4


Neogen Corporation and Subsidiaries

Consolidated Balance Sheets – Liabilities and Stockholders’ Equity

(in thousands, except shareshares and per share)

   
May 31
 
   
2021
   
2020
 
Liabilities and Stockholders’ Equity
          
Current Liabilities
          
Accounts payable
  $23,900   $25,650 
Accruals
          
Accrued compensation
   11,251    7,735 
Income taxes
   1,848    1,456 
Other accruals
   16,600    13,648 
           
Total Current Liabilities
   53,599    48,489 
   
Deferred Income Taxes
   21,917    18,125 
Other
Non-Current
Liabilities
   4,299    5,391 
           
Total Liabilities
   79,815    72,005 
   
Commitments and Contingencies (note 7)
   0    0 
   
Stockholders’ Equity
          
Preferred stock, $1.00 par value — shares authorized 100,000; NaN issued and outstanding
   0    0 
Common stock, $0.16 par value — shares authorized 120,000,000; 107,468,304 and 105,891,682 shares issued and outstanding at May 31, 2021 and 2020, respectively
   17,195    16,943 
Additional
paid-in
capital
   294,953    249,221 
Accumulated other comprehensive loss
   (11,375)   (19,709
Retained earnings
   539,604    478,722 
           
Total Neogen Corporation and Subsidiaries Stockholders’ Equity
   840,377    725,177 
  
 
 
  
 
 
 
Total Liabilities and Stockholders’ Equity
  $
 
920,192   $ 797,182 
           

 

May 31

 

 

2023

 

 

2022

 

Liabilities and Stockholders’ Equity

 

 

 

 

 

 

Current Liabilities

 

 

 

 

 

 

Accounts payable

 

$

76,669

 

 

$

34,614

 

Accrued compensation

 

 

25,153

 

 

 

11,123

 

Income tax payable

 

 

6,951

 

 

 

2,126

 

Accrued interest

 

 

11,149

 

 

 

 

Deferred revenue

 

 

4,616

 

 

 

5,460

 

Other accruals

 

 

20,934

 

 

 

24,521

 

Total Current Liabilities

 

 

145,472

 

 

 

77,844

 

Deferred Income Tax Liability

 

 

353,427

 

 

 

17,011

 

Non-Current Debt

 

 

885,439

 

 

 

 

Other Non-Current Liabilities

 

 

35,877

 

 

 

10,700

 

Total Liabilities

 

 

1,420,215

 

 

 

105,555

 

Commitments and Contingencies (note 7)

 

 

 

 

 

 

Stockholders’ Equity

 

 

 

 

 

 

Preferred stock, $1.00 par value — shares authorized 100,000; none issued
   and outstanding

 

 

 

 

 

 

Common stock, $0.16 par value — shares authorized 315,000,000; 216,245,501 and 107,801,094 shares issued and outstanding at May 31, 2023 and 2022, respectively

 

 

34,599

 

 

 

17,248

 

Additional paid-in capital

 

 

2,567,828

 

 

 

309,984

 

Accumulated other comprehensive loss

 

 

(33,251

)

 

 

(27,769

)

Retained earnings

 

 

565,041

 

 

 

587,911

 

Total Stockholders’ Equity

 

 

3,134,217

 

 

 

887,374

 

Total Liabilities and Stockholders’ Equity

 

$

4,554,432

 

 

$

992,929

 

See accompanying notes to consolidated financial statements.

F-5


Neogen Corporation and Subsidiaries

Consolidated Statements of Income

(Loss)

(in thousands, except per share)

   
Year Ended May 31
 
   
2021
   
2020
  
2019
 
Revenues
              
Product revenues
  $ 376,302   $ 335,539  $ 339,439 
Service revenues
   92,157    82,631   74,747 
   
 
 
   
 
 
  
 
 
 
Total Revenues
   468,459    418,170   414,186 
   
 
 
   
 
 
  
 
 
 
    
Cost of Revenues
              
Cost of product revenues
   201,348    173,566   179,660 
Cost of service revenues
   52,055    48,325   42,606 
   
 
 
   
 
 
  
 
 
 
Total Cost of Revenues
   253,403    221,891   222,266 
   
 
 
   
 
 
  
 
 
 
    
Gross Margin
   215,056    196,279   191,920 
    
Operating Expenses
              
Sales and marketing
   73,443    69,675   70,230 
General and administrative
   51,197    44,331   40,791 
Research and development
   16,247    14,750   12,805 
   
 
 
   
 
 
  
 
 
 
Total Operating Expenses
   140,887    128,756   123,826 
   
 
 
   
 
 
  
 
 
 
Operating Income
   74,169    67,523   68,094 
    
Other Income
              
Interest income, net
   1,614    5,992   4,683 
Royalty income
          150 
Other, net
   (515)   (1,210  32 
   
 
 
   
 
 
  
 
 
 
Total Other Income
   1,099    4,782   4,865 
   
 
 
   
 
 
  
 
 
 
Income Before Income Taxes
   75,268    72,305   72,959 
Provision for Income Taxes
   14,386    12,830   12,783 
   
 
 
   
 
 
  
 
 
 
Net Income
  $60,882   $59,475  $60,176 
   
 
 
   
 
 
  
 
 
 
Net Income per Share              
Basic
  $ 0.57   $0.57  $0.58 
Diluted
  $ 0.57   $0.56  $0.57 
Weighted Average Shares Outstanding
              
Basic
   106,499    105,100   103,776 
Diluted
   107,120    105,720   104,850 

 

Year Ended May 31

 

 

2023

 

 

2022

 

 

2021

 

Revenues

 

 

 

 

 

 

 

 

 

Product revenues, net

 

$

715,076

 

 

$

424,664

 

 

$

376,302

 

Service revenues, net

 

 

107,371

 

 

 

102,495

 

 

 

92,157

 

Total Revenues, net

 

 

822,447

 

 

 

527,159

 

 

 

468,459

 

Cost of Revenues

 

 

 

 

 

 

 

 

 

Cost of product revenues

 

 

354,707

 

 

 

228,017

 

 

 

201,348

 

Cost of service revenues

 

 

61,785

 

 

 

56,129

 

 

 

52,055

 

Total Cost of Revenues

 

 

416,492

 

 

 

284,146

 

 

 

253,403

 

Gross Margin

 

 

405,955

 

 

 

243,013

 

 

 

215,056

 

Operating Expenses

 

 

 

 

 

 

 

 

 

Sales and marketing

 

 

141,222

 

 

 

84,604

 

 

 

73,443

 

General and administrative

 

 

201,179

 

 

 

82,742

 

 

 

51,197

 

Research and development

 

 

26,039

 

 

 

17,049

 

 

 

16,247

 

Total Operating Expenses

 

 

368,440

 

 

 

184,395

 

 

 

140,887

 

Operating Income

 

 

37,515

 

 

 

58,618

 

 

 

74,169

 

Other (Expense) Income

 

 

 

 

 

 

 

 

 

Interest income

 

 

3,166

 

 

 

1,339

 

 

 

1,692

 

Interest expense

 

 

(55,961

)

 

 

(72

)

 

 

(78

)

Other, net

 

 

(6,762

)

 

 

322

 

 

 

(515

)

Total Other (Expense) Income

 

 

(59,557

)

 

 

1,589

 

 

 

1,099

 

(Loss) Income Before Taxes

 

 

(22,042

)

 

 

60,207

 

 

 

75,268

 

Provision for Income Taxes

 

 

828

 

 

 

11,900

 

 

 

14,386

 

Net (Loss) Income

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Net (Loss) Income Per Share

 

 

 

 

 

 

 

 

 

Basic

 

$

(0.12

)

 

$

0.45

 

 

$

0.57

 

Diluted

 

$

(0.12

)

 

$

0.45

 

 

$

0.57

 

Weighted Average Shares Outstanding

 

 

 

 

 

 

 

 

 

Basic

 

 

188,881

 

 

 

107,684

 

 

 

106,499

 

Diluted

 

 

188,881

 

 

 

108,020

 

 

 

107,120

 

See accompanying notes to consolidated financial statements.

F-6


Neogen Corporation and Subsidiaries

Consolidated Statements of Comprehensive Income

(Loss)

(in thousands)

   
Year Ended May 31
 
   
2021
   
2020
   
2019
 
Net Income
  $  60,882   $ 59,475   $ 60,176 
Other comprehensive income (loss), net of tax: foreign currency translations   8,602    (8,495)   (1,894
Other comprehensive income (loss), net of tax: unrealized gain on marketable securities   (268)   426    —   
                
Comprehensive income
  $69,216   $51,406   $58,282 
                

 

Year Ended May 31

 

 

2023

 

 

2022

 

 

2021

 

Net (Loss) Income

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Other comprehensive (loss) income:

 

 

 

 

 

 

 

 

 

Foreign currency translations

 

 

(4,796

)

 

 

(13,955

)

 

 

8,602

 

Unrealized gain (loss) on marketable securities, net of tax of $389, $(728), and $(80)

 

 

1,353

 

 

 

(2,439

)

 

 

(268

)

Unrealized loss on derivative instruments, net of tax of $(644)

 

 

(2,039

)

 

 

-

 

 

 

-

 

Other comprehensive (loss) income, net of tax:

 

 

(5,482

)

 

 

(16,394

)

 

 

8,334

 

Comprehensive (loss) income

 

$

(28,352

)

 

$

31,913

 

 

$

69,216

 

See accompanying notes to consolidated financial statements.

F-7


Neogen Corporation and Subsidiaries

Consolidated Statements of Stockholders’ Equity

(in thousands, except shares)

            
Accumulated
            
   
Common Stock
  
Additional
Paid-in
  
Other
Comprehensive
  
Retained
   
Non-
Controlling
   
Total
 
   
Shares
  
Amount
  
Capital
  
Income (Loss)
  
Earnings
   
Interest
   
Equity
 
Balance, June 1, 2018
  103,471,464  $ 16,555  $ 194,295   $ (9,746)  $  359,071  $
0
  
  $ 560,175 
Exercise of options and share-based compensation expense
  1,025,054   164   21,253   —     —     —     21,417 
Issuance of shares under employee stock purchase plan
  36,660   6   1,154   —     —     —     1,160 
Shares repurchased
  (100,000  (16  (3,119  —     —     —     (3,135
Net income for 2019
  —     —     —     —     60,176   0     60,176 
Other comprehensive loss
  —     —     —     (1,894  —     —     (1,894
                             
Balance, May 31, 2019
  104,433,178  $16,709  $213,583   $ (11,640)  $419,247  $0  $637,899 
Exercise of options and share-based compensation expense
  1,415,348   227   34,452   —     —     —     34,679 
Issuance of shares under employee stock purchase plan
  43,156   7   1,186   —     —     —     1,193 
Net income for 2020
  —     —     —     —     59,475   —     59,475 
Other comprehensive loss
  —     —     —     (8,069  —     —     (8,069
                             
Balance, May 31, 2020
  105,891,682  $16,943  $249,221   $ (19,709)  $478,722  $—    $725,177 
Exercise of options and share-based compensation expense
  1,410,948   226   39,454   —     —     —     39,680 
Issuance of shares under employee stock purchase plan
  38,406   6   1,382   —     —     —     1,388 
Issuance of shares for Megazyme acquisition
  
127,268
   
20
   
4,896
   
   
 
 
   
 
 
   
4,916
 
Net income for 2021
  —     —     —     0     60,882   —     60,882 
Other comprehensive gain  —     —     —     8,334   —     —     8,334 
                             
Balance, May 31, 2021
  107,468,304  $17,195  $294,953   $ (11,375)  $539,604  $—    $840,377 
                             

 

 

 

 

 

 

 

 

 

 

Accumulated

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Additional

 

 

Other

 

 

 

 

 

 

 

 

 

Common Stock

 

 

Paid-in

 

 

Comprehensive

 

 

Retained

 

 

Total

 

 

Shares

 

 

Amount

 

 

Capital

 

 

Income (Loss)

 

 

Earnings

 

 

Equity

 

Balance, June 1, 2020

 

 

105,891,682

 

 

$

16,943

 

 

$

249,221

 

 

$

(19,709

)

 

$

478,722

 

 

$

725,177

 

Exercise of options, RSUs and share-based compensation expense

 

 

1,410,948

 

 

 

226

 

 

 

39,454

 

 

 

 

 

 

 

 

 

39,680

 

Issuance of shares under employee stock purchase plan

 

 

38,406

 

 

 

6

 

 

 

1,382

 

 

 

 

 

 

 

 

 

1,388

 

Issuance of shares for Megazyme acquisition

 

 

127,268

 

 

 

20

 

 

 

4,896

 

 

 

 

 

 

 

 

 

4,916

 

Net income for 2021

 

 

 

 

 

 

 

 

 

 

 

 

 

 

60,882

 

 

 

60,882

 

Other comprehensive income

 

 

 

 

 

 

 

 

 

 

 

8,334

 

 

 

 

 

 

8,334

 

Balance, May 31, 2021

 

 

107,468,304

 

 

$

17,195

 

 

$

294,953

 

 

$

(11,375

)

 

$

539,604

 

 

$

840,377

 

Exercise of options, RSUs and share-based compensation expense

 

 

289,334

 

 

 

46

 

 

 

13,162

 

 

 

 

 

 

 

 

 

13,208

 

Issuance of shares under employee stock purchase plan

 

 

43,456

 

 

 

7

 

 

 

1,869

 

 

 

 

 

 

 

 

 

1,876

 

Net income for 2022

 

 

 

 

 

 

 

 

 

 

 

 

 

 

48,307

 

 

 

48,307

 

Other comprehensive loss

 

 

 

 

 

 

 

 

 

 

 

(16,394

)

 

 

 

 

 

(16,394

)

Balance, May 31, 2022

 

 

107,801,094

 

 

$

17,248

 

 

$

309,984

 

 

$

(27,769

)

 

 

587,911

 

 

$

887,374

 

Exercise of options, RSUs and share-based compensation expense

 

 

79,857

 

 

 

13

 

 

 

10,483

 

 

 

 

 

 

 

 

 

10,496

 

Issuance of shares under employee stock purchase plan

 

 

94,604

 

 

 

15

 

 

 

1,843

 

 

 

 

 

 

 

 

 

1,858

 

Issuance of shares for 3M transaction

 

 

108,269,946

 

 

 

17,323

 

 

 

2,245,518

 

 

 

 

 

 

 

 

 

2,262,841

 

Net loss for 2023

 

 

 

 

 

 

 

 

 

 

 

 

 

 

(22,870

)

 

 

(22,870

)

Other comprehensive loss

 

 

 

 

 

 

 

 

 

 

 

(5,482

)

 

 

 

 

 

(5,482

)

Balance, May 31, 2023

 

 

216,245,501

 

 

$

34,599

 

 

$

2,567,828

 

 

$

(33,251

)

 

$

565,041

 

 

$

3,134,217

 

See accompanying notes to consolidated financial statements.

F-8


Neogen Corporation and Subsidiaries

Consolidated Statements of Cash Flo

w
s
Flows

(in thousands)

   
Year Ended May 31
 
   
2021
   
2020
  
2019
 
Cash Flows From Operating Activities
              
Net income
  $60,882   $59,475  $60,176 
Adjustments to reconcile net income to net cash provided from operating activities:
          
Depreciation and amortization
   21,041    18,396   17,624 
Deferred income taxes
   (640)   1,601   1,197 
Share-based compensation
   6,437    6,468   5,543 
Changes in operating assets and liabilities, net of business acquisitions:
              
Accounts receivable
   (2,595)   (2,881  (4,025
Inventories
   2,450    (10,011  (10,437
Prepaid expenses and other assets
   (3,386)   (1,017  (3,569
Accounts payable
   (3,206)   6,745   (1,461
Accruals and other changes
   106    7,102   (1,206
               
Net Cash From Operating Activities
   81,089    85,878   63,842 
    
Cash Flows Used for Investing Activities              
Purchase of property, equipment and other
non-current
intangible assets
   (26,712)   (24,052  (14,661
Proceeds from the maturities of marketable securities   764,597    406,731   339,225 
Purchase of marketable securities
   (792,678)   (458,300  (437,324
Business acquisitions, net of cash acquired
   (50,771)   (13,164  (6,388
               
Net Cash Used for Investing Activitie
s
   (105,564)   (88,785  (119,148
    
Cash Flows From Financing Activities
              
Exercise of stock options and other
   34,631    29,405   17,034 
Payment of contingent consideration   (1,087)   —     —   
Repurchase of common stock   —      —     (3,135
               
Net Cash From Financing Activities
   33,544    29,405   13,899 
Effects of Foreign Exchange Rate on Cash   264    (1,917  21 
               
Net Increase (Decrease) in Cash and Cash Equivalents   9,333    24,581   (41,386
Cash and Cash Equivalents, Beginning of Year
   66,269    41,688   83,074 
               
Cash and Cash Equivalents, End of Year
  $75,602   $66,269  $41,688 
               
Supplementary Cash Flow Information
              
Income taxes paid, net of refunds
  $14,966   $7,364  $13,027 

 

Year Ended May 31

 

 

2023

 

 

2022

 

 

2021

 

Cash Flows From Operating Activities

 

 

 

 

 

 

 

 

 

Net (loss) income

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Adjustments to reconcile net (loss) income to net cash from operating activities:

 

 

 

 

 

 

 

 

 

Depreciation and amortization

 

 

88,377

 

 

 

23,694

 

 

 

21,041

 

Impairment of discontinued product lines

 

 

3,109

 

 

 

 

 

 

 

Loss on sale of minority interest and investment

 

 

2,016

 

 

 

 

 

 

 

Deferred income taxes

 

 

(19,230

)

 

 

(4,695

)

 

 

(640

)

Share-based compensation

 

 

10,177

 

 

 

7,154

 

 

 

6,437

 

Gain on disposal of property and equipment

 

 

(486

)

 

 

 

 

 

 

Amortization of debt issuance costs

 

 

2,720

 

 

 

 

 

 

 

Changes in operating assets and liabilities, net of business acquisitions:

 

 

 

 

 

 

 

 

 

Accounts receivable

 

 

(53,879

)

 

 

(7,798

)

 

 

(2,595

)

Inventories

 

 

9,955

 

 

 

(21,072

)

 

 

2,450

 

Prepaid expenses and other assets

 

 

(3,121

)

 

 

(4,054

)

 

 

(3,386

)

Accounts payable, accruals and changes

 

 

18,642

 

 

 

20,238

 

 

 

(2,221

)

Interest expense accrual

 

 

4,052

 

 

 

 

 

 

 

Changes in other non-current assets and non-current liabilities

 

 

1,566

 

 

 

6,264

 

 

 

(879

)

Net Cash From Operating Activities

 

 

41,028

 

 

 

68,038

 

 

 

81,089

 

Cash Flows From (For) Investing Activities

 

 

 

 

 

 

 

 

 

Purchase of property, equipment and other non-current intangible assets

 

 

(65,757

)

 

 

(24,429

)

 

 

(26,712

)

Proceeds from the maturities of marketable securities

 

 

266,772

 

 

 

381,839

 

 

 

764,597

 

Purchase of marketable securities

 

 

(12,523

)

 

 

(415,894

)

 

 

(792,678

)

Proceeds from the sale of property and equipment

 

 

826

 

 

 

 

 

 

 

Business acquisitions, net of working capital adjustments and cash acquired

 

 

11,721

 

 

 

(38,745

)

 

 

(50,771

)

Net Cash From (For) Investing Activities

 

 

201,039

 

 

 

(97,229

)

 

 

(105,564

)

Cash Flows (For) From Financing Activities

 

 

 

 

 

 

 

 

 

Exercise of stock options and issuance of employee stock purchase plan shares

 

 

1,195

 

 

 

7,933

 

 

 

34,631

 

Debt issuance costs paid

 

 

(19,276

)

 

 

 

 

 

 

Repayment of debt

 

 

(100,000

)

 

 

 

 

 

 

Payment of contingent consideration

 

 

 

 

 

(1,120

)

 

 

(1,087

)

Net Cash (For) From Financing Activities

 

 

(118,081

)

 

 

6,813

 

 

 

33,544

 

Effects of Foreign Exchange Rate on Cash

 

 

(5,219

)

 

 

(8,751

)

 

 

264

 

Net Increase (Decrease) in Cash and Cash Equivalents

 

 

118,767

 

 

 

(31,129

)

 

 

9,333

 

Cash and Cash Equivalents, Beginning of Year

 

 

44,473

 

 

 

75,602

 

 

 

66,269

 

Cash and Cash Equivalents, End of Year

 

$

163,240

 

 

$

44,473

 

 

$

75,602

 

Supplementary Cash Flow Information

 

 

 

 

 

 

 

 

 

Cash paid for interest

 

$

42,616

 

 

$

72

 

 

$

78

 

Income taxes paid, net of refunds

 

$

15,473

 

 

$

17,242

 

 

$

14,966

 

See accompanying notes to consolidated financial statements.

F-9


NEOGEN CORPORATION

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS

(Dollar amounts in thousands except per share and share amounts)

1.
Summary of Significant Accounting Policies
F-9

Business

Neogen Corporation and Subsidiaries

Notes to Consolidated Financial Statements
1.
Summary of Significant Accounting Policies
Nature of Operations
subsidiaries ("Neogen, Corporation develops, manufactures" "we," "our," or the "Company") develop, manufacture and marketsmarket a diverse line of products and services dedicated to food and animal safety.
Our Food Safety segment consists primarily of diagnostic test kits and complementary products (e.g., culture media) sold to food producers and processors to detect dangerous and/or unintended substances in human food and animal feed, such as foodborne pathogens, spoilage organisms, natural toxins, food allergens, genetic modifications, ruminant by-products, meat speciation, drug residues, pesticide residues and general sanitation concerns. The majority of the diagnostic test kits are disposable, single-use, immunoassay and DNA detection products that rely on proprietary antibodies and RNA and DNA testing methodologies to produce rapid and accurate test results. Our expanding line of food safety products also includes genomics-based diagnostic technology, and advanced software systems that help testers to objectively analyze and store their results and perform analysis on the results from multiple locations over extended periods.

Neogen’s Animal Safety segment is engaged in the development, manufacture, marketing and distribution of veterinary instruments, pharmaceuticals, vaccines, topicals, parasiticides, diagnostic products, rodent control products, cleaners, disinfectants, insect control products and genomics testing services for the worldwide animal safety market. The majority of these consumable products are marketed through veterinarians, retailers, livestock producers and animal health product distributors. Our line of drug detection products is sold worldwide for the detection of abused and therapeutic drugs in animals and animal products, and has expanded into the workplace and human forensic markets.

Basis of Consolidation

The consolidated financial statements include the accounts of Neogen Corporation and its subsidiaries, all of which are wholly-owned as of May 31, 2021. 

2023.

All intercompany accounts and transactions have been eliminated in consolidation.

Share and per share amounts reflect the June

4,
, 2021 2-for-1 stock split as if it took place at the beginning of the periods presented.

Functional Currency

Our functional currency is the U.S. dollar. We translate our

non-U.S.
operations’ assets and liabilities denominated in foreign currencies into U.S. dollars at current rates of exchange as of the balance sheet date and income and expense items at the average exchange rate for the reporting period. Translation adjustments resulting from exchange rate fluctuations are recorded in other comprehensive income (loss). Gains or losses from foreign currency transactions are included in other income (expense) on our consolidated statement of income.

F-10


Recently Adopted Accounting Standards

Financial Instruments—Credit Losses

Acquired contract assets and liabilities in a business combination

On June 1, 2020,2023, the Company adopted ASU No.

2016-13—Measurement
2021-08, Business Combinations (Topic 805): Accounting for Contract Assets and Contract Liabilities from Contracts with Customers, which amended ASC 805 to require an acquirer to, at the date of Credit Losses on Financial Instruments, which changes howacquisition, recognize and measure contract assets and contract liabilities acquired in accordance with ASU 2014-09, Revenue from Contracts with Customers (Topic 606) as if the Company measures credit losses on most financial instruments measured at amortized cost and certain other instruments, such as loans, receivables and
held-to-maturity
debt securities. Rather than generally recognizing credit losses when it is probable thatentity had originated the loss has been incurred, the revised guidance requires the Company to recognize an allowance for credit losses for the difference between the amortized cost basis of a financial instrument and the amount of amortized cost that the Company expects to collect over the instrument’s contractual life. The adoptioncontracts. Adoption of this guidancestandard did not have a material impact on ourits consolidated financial statements due to the Company’s short-term contractual life of receivables and minimal expected losses.
Fair Value Measurements
related disclosures.

Reference Rate Reform

On JuneSeptember 1, 2020,2022, the Company adopted ASU

2018-13,
Fair Value Measurement (Topic 820): Disclosure Framework-Changes to the Disclosure Requirements for Fair Value Measurement, which modifies the disclosure requirements of fair value measurements. The adoption of this guidance did not have an impact on our consolidated financial statements.
Cloud Computing Implementation Cost
On June 1, 2020, the Company adopted ASU
2018-15,
Intangible-Goodwill and Other
Internal-Use
Software (Subtopic
350-40):
Customer’s Accounting for Implementation Cost Incurred in a Cloud Computing Arrangement That Is a Service Contract, which clarifies the accounting for implementation costs in cloud computing arrangements. The adoption of this guidance did not have an impact on our consolidated financial statements.
F-10

Recent Accounting Pronouncements Not Yet Adopted
Reference Rate Reform
In March 2020, FASB issued Update
2020-04,
Standards Codification Topic 848, Reference Rate Reform (Topic(Topic 848): Facilitation of the Effects of Reference Rate Reform on Financial Reporting. This update provides, which provided temporary optional expedients to applying the reference rate reform guidance to contracts that reference LIBOR or another reference rate expected to be discontinued. Under this update,Topic 848, contract modifications resulting infrom the transition to a new reference rate may be accounted for as a continuation of the existing contract. This guidance is effective upon issuanceThe Company now uses the Secured Overnight Financing Rate (SOFR). Adoption of the update and applies to contract modifications made through December 31, 2022. We will adopt this standard when LIBOR is discontinued. We are evaluating thedid not have a material impact the new standard will have on ourits consolidated financial statements and related disclosures but do not anticipate a material impact.disclosures.

Income Tax Simplification
In December 2019, the Financial

Accounting Standards Board (“FASB”) issued UpdatePolicies

2019-12,
Income Taxes (“Topic 740”) as part of its Simplification Initiative. This guidance provides amendments to simplify the accounting for income taxes by removing certain exceptions to the general principles in Topic 740. The amendments also improve consistent application of and simplify GAAP for other areas of Topic 740 by clarifying and amending existing guidance. This guidance is effective for annual and interim reporting periods beginning after December 15, 2020, and early adoption is permitted. We plan to adopt during the first quarter of 2021, and we expect an immaterial impact to our consolidated financial statements.
Comprehensive Income
Comprehensive income represents net income and any revenues, expenses, gains and losses that, under U.S. generally accepted accounting principles, are excluded from net income and recognized directly as a component of stockholders’ equity. Accumulated other comprehensive income (loss) consists of foreign currency translation adjustments and unrealized gains and losses on our marketable securities.
Changes in our Accumulated Other Comprehensive Income (Loss) (“AOCI”) balances, net of tax, were as follows:
(in thousands)
  
Foreign Currency
Translation Adjustments
  
Unrealized Gain on
Marketable Securities
  
        Total AOCI        
 
Balance, May 31, 2019
  $(11,640 $—    $(11,640
Other comprehensive income (loss)
   (8,495  426   (8,069
   
 
 
  
 
 
  
 
 
 
Balance, May 31, 2020
  $(20,135 $426  $(19,709
Other comprehensive income (loss)
   8,602   (268  8,334 
   
 
 
  
 
 
  
 
 
 
Balance, May 31, 2021
  $(11,533 $158  $(11,375
   
 
 
  
 
 
  
 
 
Fair Value of Financial Instruments
The carrying amounts of the Company’s financial instruments other than cash equivalents and marketable securities, which include accounts receivable and accounts payable, approximate fair value based on either their short maturity or current terms for similar instruments.
Fair value measurements are determined based upon the exit price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants exclusive of any transaction costs. The Company utilizes a fair value hierarchy based upon the observability of inputs used in valuation techniques as follows:
F-11

Level 1:
Observable inputs such as quoted prices in active markets;
Level 2:
Inputs, other than quoted prices in active markets, that are observable either directly or indirectly; and
Level 3:
Unobservable inputs in which there is little or no market data, which require the reporting entity to develop its own assumptions.

Cash and Cash Equivalents

Cash and cash equivalents consist of bank demand accounts, savings deposits, certificates of deposit and commercial paper with original maturities of 90 days or less. Cash and cash equivalents are maintained at financial institutions and, at times, balances may exceed federally insured limits. The Company has not experienced losses related to these balances and believes it is not exposed to significant credit risk regarding its cash and cash equivalents. Cash and cash equivalents were $75,602,000 and $66,269,000 at May 31, 2021 and 2020, respectively. The carrying value of these assets approximates fair value due to the short maturity of these instruments and is classified as Level 1 in the fair value hierarchy. Cash held by foreign subsidiaries was $15,246,000$36,288 and $13,060,000$17,057 at May 31, 20212023 and 2020,2022, respectively.

Marketable Securities

The Company has marketable securities held by banks or broker-dealers at May 31, 2021, consisting of short-term domestic certificates of deposit of $5,785,000

and commercial paper and corporate bonds rated at least A-1/P-1 (short-term) and A/A2 (long-term) with original maturities between
91 days and two years of $299,700,000. Total outstanding marketable. These securities at May 31, 2021 were $305,485,000; there were $277,404,000
in marketable securities outstanding at May 31, 2020.are classified as available for sale. Changes in marketfair value are monitored and recorded on a monthly basis;basis and are recorded in other comprehensive income (loss). In the event of a downgrade in credit quality subsequent to purchase, the marketable securitysecurities investment is evaluated to determine the appropriate action to take to minimize the overall risk to our marketable securitysecurities portfolio. As these securities are highly rated and short-term in nature, they have very little credit risk; therefore,If fair value is less than its amortized cost basis, then the Company does not believeevaluates whether the decline is the result of a reservecredit loss, in which case an impairment is recorded through an allowance for expected credit losses on marketable securitieslosses. Where there is material. These securities are classified as available for sale.an intention or a requirement to sell an impaired available-for-sale debt security, the entire impairment is recognized in earnings with a corresponding adjustment to the amortized cost basis of the security. The primary objective of management’s short-term investment activity is to preserve capital for the purpose of funding current operations, capital expenditures and business acquisitions; short-termacquisitions. Short-term investments are not entered into for trading or speculative purposes. These securities are recorded at fair value based on recent trades or pricing models and therefore meet the Level 2 criteria. Interest income on these investments is recorded within other (expense) income on ourthe consolidated statements of income. Adjustments in the fair value of these assets are recorded in other comprehensive income.
income (loss).

F-11


Marketable Securities as of May 31, 20212023 and 20202022 are listed below by classification and remaining maturitiesmaturities.

 

 

 

Year ended May 31

 

 

 

Maturity

 

2023

 

 

2022

 

Commercial Paper & Corporate Bonds

 

0 - 90 days

 

$

22,552

 

 

$

106,497

 

 

91 -180 days

 

 

35,692

 

 

 

61,373

 

 

181 days -1 year

 

 

23,768

 

 

 

91,706

 

 

1 - 2 years

 

 

317

 

 

 

77,002

 

Total Marketable Securities

 

 

 

$

82,329

 

 

$

336,578

 

.
      
Year ended May 31
 
(in thousands)
  
Maturity
  
2021
   
2020
 
US Treasuries
  
0 - 90
days
  $0     $—   
   
91 -180
 days
   0      —   
   181 days - 1 year   0      2,532 
   1 - 2 years   0      —   
           
Commercial Paper & Corporate Bonds
  0 - 90 days   106,631    133,130 
   
91 - 180 days
   78,727    73,824 
   
181 days - 1 year
   87,590    43,231 
    1 - 2 years    26,752    7,839 
           
Certificates of Deposit
  0 - 90 days   3,262    1,003 
   
91 - 180 days
   1,260    5,184 
   
181 days - 1 year
   1,263    6,069 
   1 - 2 years   0      4,592 
              
Total Marketable Securities
  $305,485   $277,404 
           
F-12

The components of marketable securities
as of
May 31, 2021 are as follows:
(in thousands)
  
Amortized

Cost
   
Unrealized

Gains
   
Unrealized

Losses
   
Fair Value
 
US Treasuries
  $0     $0     $0     $0   
Commercial Paper & Corporate Bonds
   299,524    209    (33)     299,700 
Certificates of Deposit
   5,755    30    0      5,785 
                     
Total Marketable Securities
  $305,279   $239   $(33)    $305,485 
                     

The components of marketable securities as of May 31, 20202023 are as follows:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Amortized
Cost

 

 

Unrealized
Gains

 

 

Unrealized
Losses

 

 

Fair Value

 

Commercial Paper & Corporate Bonds

 

$

83,549

 

 

$

0

 

 

$

(1,220

)

 

$

82,329

 

The components of marketable securities as of May 31, 2022 are as follows:

 

 

Amortized
Cost

 

 

Unrealized
Gains

 

 

Unrealized
Losses

 

 

Fair Value

 

Commercial Paper & Corporate Bonds

 

$

339,540

 

 

$

7

 

 

$

(2,969

)

 

$

336,578

 

Derivative Financial Instruments

The Company operates on a global basis and is exposed to the risk that its financial condition, results of operations and cash flows could be adversely affected by changes in foreign currency exchange rates and changes in interest rates. To reduce the potential effects of foreign currency exchange rate movements on net earnings, the Company enters into derivative financial instruments in the form of foreign currency exchange forward contracts with major financial institutions and have also entered into interest rate swap contracts as a hedge against changes in interest rates. The Company has established policies and procedures for risk assessment and the approval, reporting and monitoring of derivative financial instrument activities. On the date the derivative is established, the Company designates the derivative as either a fair value hedge, a cash flow hedge or a net investment hedge in accordance with its established policy. Each reporting period, derivatives are recorded at fair value in other current assets, other assets, accrued liabilities and other long-term liabilities. The change in fair value is recorded in accumulated other comprehensive income (loss), and amounts are reclassified into earnings on the consolidated statement of income (loss) when transactions are realized. Derivatives that are not determined to be effective hedges are adjusted to fair value with a corresponding adjustment to earnings. The Company does not enter into derivative financial instruments for trading or speculative purposes.

(in thousands)
  
Amortized
Cost
   
Unrealized
Gains
   
Unrealized
Losses
   
Fair Value
 
US Treasuries
  $2,502   $30   $0     $2,532 
Commercial Paper & Corporate Bonds
   257,700    347    (23   258,024 
Certificates of Deposit
   16,648    200    0      16,848 
   
 
 
   
 
 
   
 
 
   
 
 
 
Total Marketable Securities
  $276,850   $577   $(23  $277,404 
   
 
 
   
 
 
   
 
 
   
 
 
 

Use of Estimates

The preparation of these consolidated financial statements in conformity with U.S. GAAP requires that management to make estimates and judgments that affect amounts reflected in the reported amountsconsolidated financial statements. Considerable judgment is often involved in making such estimates, and the use of assets, liabilities, revenuesdifferent assumptions could result in different conclusions. Management believes its assumptions and expenses, and related disclosures of contingent assets and liabilities. On an ongoing basis, management evaluates the estimates, including, but not limited to, variable consideration related to revenue recognition, allowances for doubtful accounts, the market value of, and demand for, inventories, stock-based compensation, provision for income taxes and related balance sheet accounts, accruals, goodwill and other intangible assets

. We believe that these estimates have the greatest potential impact on our financial statements, so we consider them to be our critical accounting policies and estimates. These estimates are based on historical experiencereasonable and on various other assumptions that are believed to be reasonable under the circumstances, theappropriate. However, actual results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Though the impact of the
COVID-19
pandemic to our business and operating results presents additional uncertainty, we continue to use the best information available to inform our critical accounting estimates. Actual results maycould differ from these estimates under different assumptions or conditions.those estimates.

Accounts Receivable and Concentrations of Credit Risk

Financial instruments which potentially subject Neogen to concentrations of credit risk consist principally of accounts receivable. Management attempts to minimize credit risk by reviewing customers’ credit histories before extending credit and by monitoring credit exposure on a regular basis. Collateral or other security is generally not required for accounts receivable. We maintain an allowance for customer accounts that reduces receivables to amounts that are expected to be collected. In estimating the allowance for doubtful accounts,credit losses, management considers relevant information about past events, current conditions and reasonable and supportable forecasts that affect the collectability of financial assets. Once a receivable balance has been determined to be uncollectible, generally after all collection efforts have been exhausted, that

F-12


amount is charged against the allowance for doubtful accounts.credit losses. No customer accounted for more than

 10%
10% of accounts receivable at May 31, 20212023 or 2020,2022, respectively. The activity in the allowance for doubtful accountscredit losses was as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Beginning Balance

 

$

1,650

 

 

$

1,400

 

 

$

1,350

 

Provision

 

 

1,460

 

 

 

332

 

 

 

239

 

Recoveries

 

 

46

 

 

 

98

 

 

 

139

 

Write-offs

 

 

(329

)

 

 

(180

)

 

 

(328

)

Ending Balance

 

$

2,827

 

 

$

1,650

 

 

$

1,400

 

Inventories

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
   
2019
 
Beginning Balance
  $1,350   $1,700   $1,550 
Provision
   239    393    263 
Recoveries
   139    49    38 
Write-offs
   (328)     (792)   (151
                
Ending Balance
  $1,400   $1,350   $1,700 
                
F-13

Inventories

Inventories are stated at the lower of cost or net realizable value, determined on the

first-in,
first-out
method. The components of inventories were as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

Raw Materials

 

$

64,971

 

 

$

58,667

 

Work-in-process

 

 

5,369

 

 

 

6,388

 

Finished goods

 

 

63,472

 

 

 

57,258

 

 

$

133,812

 

 

$

122,313

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
 
Raw Materials
  $47,588   $45,058 
Work-in-process
   6,412    6,887 
Finished goods
   46,701    43,108 
           
   $100,701   $95,053 
           

The Company’s inventories are analyzed for slow moving, expired and obsolete items on a quarterly basis and the valuation allowance is adjusted as required within cost of salesrevenues expense. The valuation allowance for inventory was $3,100,000$6,270 and $2,850,000$4,050 at May 31, 20212023 and 2020,2022, respectively.

Property and Equipment

Property and equipment is stated at cost. Expenditures for major improvements are capitalized while repairs and maintenance are charged to expense as incurred. Depreciation is provided on the straight-line method over the estimated useful lives of the respective assets, which are generally sevento 39 years for buildings and improvements, and three to ten10 years for furniture, fixtures, computers, leasehold improvements, and machinery and equipment. Depreciation expense was $13,288,000, $11,907,000$17,292, $14,094, and $11,315,000$13,288 in fiscal years 2023, 2022, and 2021, 2020 and 2019, respectively.

Goodwill and Other Intangible Assets

Goodwill represents the excess of purchase price over fair value of tangible net assets of acquired businesses after amounts are allocated to other identifiable intangible assets. The Company's business is organized into two operating segments: Food Safety and Animal Safety. Under the goodwill guidance, management determined that each of its segments represents a reporting unit. Other intangible assets include customer relationships, trademarks, licenses, trade names, covenants

not-to-compete
and patents. Amortizable intangible assetsCustomer relationships intangibles are amortized on either an accelerated or straight-line basis, reflecting the pattern in which the economic benefits are consumed, while all other amortizable intangibles are amortized on a straight-line basis, generallybasis. Intangibles are amortized over 52 to 25 years.

Management reviews the carrying amounts of goodwill and other

annually at the reporting unit level, or when indications of impairment exist, to determine if goodwill may be impaired. Goodwill is tested for impairment annually in the fourth quarter. Management also reviews the carrying amounts of non-amortizable
intangible assets annually, or when indications of impairment exist, to determine if such assets may be impaired. In evaluating goodwillThese are tested for impairment we have the option to first assess the qualitative factors to determine whether it is more likely than not that the fair value of the reporting unit is less than its carrying amount as a basis for determining whether it is necessary to perform the goodwill impairment test. In contrast, we can opt to bypass the qualitative assessment for any reporting unitannually in any period and proceed directly to assessing the fair value of all of our reporting units and compare the fair value of the reporting unit to carrying value to determine if any impairment is necessary. Doing so does not preclude us from performing the qualitative assessment in any subsequent period. In the fourth quarterquarter. During management's annual test or when there are indicators of fiscal
2021
, we elected to bypass the qualitative approach that allows the assessment of qualitative factors to determine whether it is more likely than not that the fair value of a reporting unit is less than its carrying amount and instead proceeded directly to assessing the fair value of all of our reporting units and comparing the fair values of the reporting units to the carrying values to determineimpairment, if any impairment is necessary.
If the carrying amounts of these assets are deemed to be less than fair value based upon a discounted cash flow analysis and comparison to comparable earnings

F-13


EBITDA multiples of peer companies, such assets are reduced to their estimated fair value and a charge is maderecorded to operations. NaN goodwill impairments were identified during

Amortizable intangible assets are tested for impairment when indications of impairment exist. If the years ended May 31, 2021, 2020carrying amounts of these assets are deemed to be less than fair value based upon a discounted cash flow analysis, such assets are reduced to their estimated fair value and 2019, respectively. The remaining weighted-average amortization period for intangibles was 10 years and 9 years at May 31, 2021 and May 31, 2020, respectively.a charge is recorded to operations.

F-14


Long-lived Assets

Management reviews the carrying values of its long-lived assets to be held and used, including definite-lived intangible assets, for possible impairment whenever events or changes in business conditions warrant such a review. The carrying value of a long-lived asset is considered impaired when the anticipated separately identifiable undiscounted cash flows over the remaining useful life of the asset are less than the carrying value of the asset. In such an event, fair value is determined using discounted cash flows, and if lower than the carrying value, impairment is recognized through a charge to operations. NaNNo impairments of long-lived assets were identified during the years ended May 31, 2023, 2022 and 2021, 2020 and 2019, respectively.

Reclassifications
Certain immaterial amounts in the fiscal 2020 and 2019 consolidated financial statements have been reclassified to conform with the fiscal 2021 presentation.
Equity

Equity Compensation Plans

At May 31, 2021,2023, the Company had stock option plans which are described more fully in Note 5 to the consolidated financial statements.

We measure stock-based compensation at the grant date, based on the estimated fair value of the award, and recognize the cost (net of estimated forfeitures) as compensation expense on a straight-line basis over the requisite service period. Our stock-based compensation expense is reflected in general and administrative expense in our consolidated statements of income.​​​​​​​

income (loss).

The weighted-average fair value per share of stock options granted during fiscal years 2021, 2020 and 2019, estimated on the date of grant using the Black-Scholes option pricing model, was $7.71, $7.78 and $7.46, respectively. The fair value of stock options granted was estimated using the following weighted-average assumptions:
   
Year ended May 31
 
   
2021
  
2020
  
2019
 
Risk-free interest rate
   0.2%  1.9  2.6
Expected dividend yield
   0.0%  0.0  0.0
Expected stock volatility
   31.3%  29.4  27.0
Expected option life
   3.25 years   3.5 years   3.5 years 
The risk-free interest rate for periods within the expected life of options granted is based on the United States Treasury yield curve in effect at the time of grant. Expected stock price volatility is based on historical volatility of the Company’s stock. The expected option life, representing the period of time that options granted are expected to be outstanding, is based on historical option exercise and employee termination data. We include recent historical experience in estimating our forfeitures. As employees terminate, grant tranches expire or as forfeitures are known, estimated expense is adjusted to actual. For options granted in fiscal years 2021, 2020 and 2019, the Company recorded charges in general and administrative expense based on the fair value of stock options using the straight-line method over the vesting period, generally five years.
The Company also issues restricted stock units (RSUs), which are described more fully in Note 5 to the consolidated financial statements. The RSUs generally vest over

three to five years and have a weighted average value of $34.21 in fiscal 2021, which was the first year this type of award was issued.

Income Taxes
We account for income taxes using the asset and liability method. Under this method, deferred income tax assets and liabilities are determined based on differences between the financial reporting and tax bases of assets and liabilities and for tax credit carryforwards and are measured using the enacted tax rates in effect for the years in which the differences are expected to reverse. Deferred income tax expense represents the change in net deferred income tax assets and liabilities during the year.
F-15

Our wholly-owned foreign subsidiaries are comprised of Neogen Europe, Quat-Chem Ltd, Megazyme Ltd, Megazyme IP, Neogen Italia S.r.l., Neogen do Brasil, Rogama Industria e Comercio Ltda, Neogen Latinoamérica, Neogen Argentina, Neogen Uruguay, Neogen Chile SpA, Neogen
Bio-Scientific
Technology Co (Shanghai), Neogen Food and Animal Security (India), Neogen Canada, and Neogen Australasia Pty Limited. Based on historical experience, as well as management’s future plans, earnings from these subsidiaries are expected to be
re-invested
indefinitely for future expansion and working capital needs. Furthermore, our domestic operations have historically produced sufficient operating cash flow to mitigate the need to remit foreign earnings. On an annual basis, we evaluate the current business environment and whether any new events or other external changes might require a
re-evaluation
of the decision to indefinitely
re-invest
foreign earnings. It is not practicable to determine the income tax liability that would be payable if such earnings were not reinvested indefinitely.
Research and Development Costs

Research and development costs, which consist primarily of compensation costs, administrative expenses and new product development, among other items, are expensed as incurred.

Advertising Costs

Advertising costs are expensed within sales and marketing as incurred and totaled $1,687,000, $1,454,000$2,548, $2,018, and $1,471,000$1,687 in fiscal years 2023, 2022, and 2021, 2020 and 2019, respectively.

Net (Loss) Income per Share

Basic net (loss) income per share is based on the weighted average number of common shares outstanding during each year. Diluted (loss) earnings per share is based on the weighted average number of common shares and dilutive potential common shares outstanding. Our dilutive potential common shares outstanding during the years result entirely from dilutive stock options. options and restricted stock units. The following table presents the net (loss) income per share calculations:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Numerator for basic and diluted net (loss) income per share — Net (Loss) Income

 

$

(22,870

)

 

$

48,307

 

 

$

60,882

 

Denominator for basic net (loss) income per share — Weighted average shares

 

 

188,881

 

 

 

107,684

 

 

 

106,499

 

Effect of dilutive stock options and restricted stock units

 

 

-

 

 

 

336

 

 

 

621

 

Denominator for diluted net (loss) income per share

 

 

188,881

 

 

 

108,020

 

 

 

107,120

 

Net (loss) income attributable per share

 

 

 

 

 

 

 

 

 

Basic

 

$

(0.12

)

 

$

0.45

 

 

$

0.57

 

Diluted

 

$

(0.12

)

 

$

0.45

 

 

$

0.57

 

   
Year ended May 31
 
(in thousands, except per share)
  
2021
   
2020
   
2019
 
Numerator for basic and diluted net income per share — Net Income
  $60,882   $ 59,475   $ 60,176 
             
Denominator for basic net income per share — Weighted average shares
   106,499    105,100    103,776 
Effect of dilutive stock options
   621    620    1,074 
                
Denominator for diluted net income per share
   107,120    105,720    104,850 
Net income attributable to Neogen per share
               
Basic
  $0.57   $0.57   $0.58 
Diluted
  $0.57   $0.56   $0.57 

F-14


Due to the net loss in fiscal 2023, the dilutive stock options and RSUs are anti-dilutive. At May 31, 2023 and May 31, 2022, 148,000 and 383,000 shares, respectively, were excluded from the calculation of diluted net (loss) income per share, because the inclusion of such securities in the calculation would have been anti-dilutive. At May 31, 2021, 0 potential shares from option exercises were excluded from the computation of diluted net income per share, as the option exercise

prices did not exceed the average market price of the common shares. 
At May 31, 2020, 56,000no potential shares were excluded from the computation. At May 31, 2019, 10,000 potential shares were excluded from the computation.

Leases

On June 1, 2019, we adopted Topic 842 using the prospective approach and did not retrospectively apply to prior periods. Topic 842 requires the

The Company to recognizerecognizes in the statement of financial position a liability to make lease payments (the lease liability) and a

right-of-use
asset representing its right to use the underlying asset for the lease term. Upon adoption of Topic 842, weWe recognized all leases with terms greater than 12 months in duration on our consolidated balance sheets as
right-of-use
assets and lease liabilities of approximately $2.0 million.
. Right-of-use
assets are recorded in other assets on our consolidated balance sheets. Current and
non-current
lease liabilities are recorded in other accruals within current liabilities and other
non-current
liabilities, respectively, on our consolidated balance sheets. The recognition, measurement and presentation of expenses and cash flows arising from a lease by a lessor have not significantly changed from previous U.S. GAAP.
F-16

We lease various manufacturing, laboratory, warehousing and distribution facilities, administrative and sales offices, equipment and vehicles under operating leases. We evaluate our contracts to determine if an arrangement is a lease at inception and classify it as a finance or operating lease. Currently, all of our leases are classified as operating leases. Leased assets and corresponding liabilities are recognized based on the present value of the lease payments over the lease term. Our lease terms may include options to extend when it is reasonably certain that we will exercise that option.

We have made certain assumptions and judgments when applying ASC 842,accounting for leases, the most significant of which are:

We elected the package of practical expedients available for transition that allow us to not reassess
:
whether expired or existing contracts contain leases under the new definition of a lease, lease classification for expired or existing leases
,
and whether previously capitalized initial direct costs would qualify for capitalization under ASC 842.
We did not elect to use hindsight when considering judgments and estimates such as assessments of lessee options to extend or terminate a lease or purchase the underlying asset.
For all asset classes, we elected to not recognize a
right-of-use
asset and lease liability for short-term leases (i.e. leases with a term of 12 months or less).
For all asset classes, we elected to not separate
non-lease
components from lease components to which they relate and have accounted for the combined lease and
non-lease
components as a single lease component.
The determination of the discount rate used in a lease is our incremental borrowing rate that is based on our estimate of what we would normally pay to borrow on a fully collateralized and amortized basis over a similar term an amount equal to the lease payments.

Supplemental balance sheet information related to operating leases was as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

Rights of use - assets

 

$

11,933

 

 

$

3,184

 

Lease liabilities - current

 

 

3,277

 

 

 

1,440

 

Lease liabilities - non-current

 

 

8,812

 

 

 

1,788

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
 
Rights of use—assets
  $2,477   $ 1,952 
Lease liabilities—current
   1,285    1,054 
Lease liabilities—non-current
   1,207    913 

The weighted average remaining lease term and weighted average discount rate were as follows:

 

Year ended May 31

 

 

2023

 

 

2022

 

Weighted average remaining lease term

 

4.7 years

 

 

3 years

 

Weighted average discount rate

 

 

4.7

%

 

 

1.7

%

   
Year ended May 31
 
   
2021
  
2020
 
Weighted average remaining lease term
   2 years   2.5 years 
Weighted average discount rate
   2.0%   3.2% 

Operating lease expenses are classified as cost of revenues or operating expenses on the consolidated statements of income. income (loss). The components of lease expense were as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

Operating leases

 

$

2,097

 

 

$

438

 

Short term leases

 

 

460

 

 

 

277

 

Total lease expense

 

$

2,557

 

 

$

715

 

F-15


   
Year ended May 31
 
(in thousands)
  
2021
   
2020
 
Operating leases
  $1,352   $ 1,207 
Short term leases
   134    166 
Total lease expense
  $1,486   $1,373 
 
 
 
 
 
 
 
 
 
F-17

Cash paid for amounts included in the measurement of lease liabilities for operating leases included in cash flows from operations on the statement of cash flows was approximately $1,397,000,

 $1,178,000
$2,139, $1,407, and $1,633,000$1,397 for the years ended May 31, 2023, 2022 and 2021, 2020 and 2019, respectively. There were
0
non-cash
Non-cash additions to
right-of-use
assets obtained from new operating lease liabilities were $11,192for the year ended May 31, 2021.
2023.

Maturities of operating lease liabilities as of May 31, 20212023 are as follows:

Years ending May 31,

 

Amount

 

2024

 

$

3,542

 

2025

 

 

3,014

 

2026

 

 

2,725

 

2027

 

 

1,624

 

2028

 

 

1,105

 

2029 and thereafter

 

 

1,885

 

Total lease payments

 

$

13,895

 

Less: imputed interest

 

 

(1,806

)

Total lease liabilities

 

$

12,089

 

(in thousands)
  
Amount
 
Years ending May 31, 202
2
  $ 1,313 
2023
   874 
2024
   345 
2025
   42 
2026
and thereafter
   0 
      
Total lease payments
  $2,574 
Less: imputed interest
   (82)
      
Total lease liabilities
  $2,492 
      

Revenue Recognition

We determine the amount of revenue to be recognized through application of the following steps:

Identification of the contract with a customer;
Identification of the performance obligations in the contract;
Determination of the transaction price;
Allocation of the transaction price to the performance obligations in the contract; and
Recognition of revenue when or as the Company satisfies the performance obligations.

Essentially all of Neogen’s revenue is generated through contracts with its customers. A performance obligation is a promise in a contract to transfer a product or service to a customer. We generally recognized revenue at a point in time when all of our performance obligations under the terms of a contract are satisfied. Revenue is recognized upon transfer of control of promised products or services in an amount that reflects the consideration we expect to receive in exchange for those products or services. The collectability of consideration on the contract is reasonably assured before revenue is recognized. To the extent that customer payment has been received before all recognition criteria are met, these revenues are initially deferred in other accruals on the balance sheet and the revenue is recognized in the period that all recognition criteria have been met.

Certain agreements with customers include discounts or rebates on the sale of products and services applied retrospectively, such as volume rebates achieved by purchasing a specified purchase threshold of goods and services. We account for these discounts as variable consideration and estimate the likelihood of a customer meeting the threshold in order to determine the transaction price using the most predictive approach. We typically use the most-likely-amount method, for incentives that are offered to individual customers, and the expected-value method, for programs that are offered to a broad group of customers. Variable consideration reduces the amount of revenue that is recognized. Rebate obligations related to customer incentive programs are recorded in accrued liabilities; theliabilities. The rebate estimates are adjusted at the end of each applicable measurement period based on information currently available.

F-18

The performance obligations in Neogen’s contracts are generally satisfied well within one year of contract inception. In such cases, management has elected the practical expedient to not adjust the promised amount of consideration for the effects of a significant financing component. Management has elected to utilize the practical expedient to recognize the incremental costs of obtaining a contract as an expense when incurred because the amortization period for the prepaid costs that would otherwise have been deferred and amortized is one year or less. We account for shipping and handling for products as a fulfillment activity when goods are shipped. Shipping and handling costs that are charged to and reimbursed

F-16


by the customer are recognized as revenues, while the related expenses incurred by Neogen are recorded in sales and marketing expense; theseexpense. These expenses totaled $15,180,000, $13,514,000$18,513, $17,482, and $13,503,000$15,180 in fiscal years 2021, 20202023, 2022, and 2019,2021, respectively. Revenue is recognized net of any tax collected from customers; thecustomers. The taxes are subsequently remitted to governmental authorities. Our terms and conditions of sale generally do not provide for returns of product or reperformance of service except in the case of quality or warranty issues. TheseWhile these situations are infrequent;infrequent, due to immateriality of the amount, warranty claims are recorded in the period incurred.​​​​​​​

The Company derives revenue from two primary sources — product revenue and service revenue.

Product revenue consists primarily of shipments of:

Diagnostic test kits, culture media and related products used by food producers and processors to detect harmful natural toxins, foodborne bacteria, allergens and levels of general sanitation;
Consumable products marketed to veterinarians, retailers, livestock producers and animal health product distributors; and
Rodenticides,Rodent control products, disinfectants and insecticidesinsect control products to assist in the control of rodents, insects and disease in and around agricultural, food production and other facilities.

Revenue for Neogen’s products are recognized and invoiced when the product is shipped to the customer.

Service revenue consists primarily of:

Genomic identification and related interpretive bioinformatic services; and
Other commercial laboratory services.

Revenues for Neogen’s genomics and commercial laboratory services are recognized and invoiced when the applicable laboratory service is performed and the results are conveyed to the customer.

Payment terms for products and services are generally 30 to 60 days.

F-19

performance obligation(s) and recognition of revenue. Upon completion of the performance obligation(s) that the Company has with the customer, the liability for the customer deposit is relieved and revenue is recognized. These customer deposits are listed as Deferred revenue on the consolidated balance sheets. During fiscal year 2023 and 2022, the Company recorded additions of $11,046 and $10,229 to deferred revenue, respectively. During fiscal year 2023 and 2022, the Company recognized $11,890 and $8,173, respectively, of deferred revenue amounts into revenue. Changes in the balances relate primarily to sales of the Company's genomics services.

On September 1, 2022, Neogen closed on a Reverse Morris Trust transaction to combine with 3M’s Food Safety business. Similar to Neogen, 3M’s former Food Safety business sells diagnostic test kits, dehydrated culture media, and related products used by food producers and processors to detect foodborne bacteria, allergens and levels of general sanitation. Revenue for these products are recognized and invoiced when the product is shipped to the customer. These products are currently manufactured, invoiced and distributed by 3M on behalf of, and as directed by Neogen to its customers under a number of transition service contracts.

F-17


The following table presents disaggregated revenue by major product and service categories for the years ended May 31, 2021, 20202023, 2022 and 2019:2021:

Year Ended

 

 

May 31, 2023

 

May 31, 2022

 

May 31, 2021

 

Food Safety:

 

 

 

 

 

 

Natural Toxins, Allergens & Drug Residues

$

82,567

 

$

79,395

 

$

76,614

 

Bacterial & General Sanitation

 

134,934

 

 

47,282

 

 

44,009

 

Culture Media & Other

 

267,178

 

 

75,278

 

 

61,245

 

Rodent Control, Insect Control & Disinfectants

 

39,655

 

 

35,691

 

 

32,219

 

Genomics Services

 

22,463

 

 

22,333

 

 

20,157

 

$

546,797

 

$

259,979

 

$

234,244

 

Animal Safety:

 

 

 

 

 

 

Life Sciences

 

6,254

 

 

5,685

 

 

5,715

 

Veterinary Instruments & Disposables

 

63,843

 

 

63,938

 

 

48,128

 

Animal Care & Other

 

39,068

 

 

39,805

 

 

35,897

 

Rodent Control, Insect Control & Disinfectants

 

87,423

 

 

83,610

 

 

77,458

 

Genomics Services

 

79,062

 

 

74,142

 

 

67,017

 

$

275,650

 

$

267,180

 

$

234,215

 

Total Revenue

$

822,447

 

$

527,159

 

$

468,459

 

2.
Goodwill and Other Intangible Assets
   
Year Ended
 
(dollars in thousands)
  
May 31, 2021
   
Change
  
May 31, 2020
   
Change
  
May 31, 2019
 
Food Safety:
                       
      
Natural Toxins, Allergens & Drug Residues
  $76,614    1 $76,207    (3%) $78,373 
Bacterial & General Sanitation
   44,009    5  41,780    (0%)  41,966 
Culture Media & Other
   56,922    19  47,847    (4%)  49,857 
Rodenticides, Insecticides & Disinfectants
   36,542    26  28,890    13  25,584 
Genomics Services
   20,157    12  17,967    2  17,694 
                        
   $234,244    10 $212,691    (0%) $213,474 
Animal Safety:
                       
      
Life Sciences
   5,715    (10%
)
 
  6,322    (20%)   7,858 
Veterinary Instruments & Disposables
   48,128    12  42,941    (4%)   44,582 
Animal Care & Other
   35,897    26  28,389    (5%)   29,941 
Rodenticides, Insecticides & Disinfectants
   77,458    13  68,815    4  66,389 
Genomics Services
   67,017    14  59,012    14  51,942 
                        
   $234,215    14 $205,479    2 $200,712 
                        
Total Revenue
  $468,459    12 $418,170    1 $414,186 
                        
See Note 9 to the consolidated financial statements for disaggregated revenues by geographical location.
2.
Goodwill and Other Intangible Assets

Goodwill

Management completed the annual impairment analysis of goodwill and intangible assets with indefinite lives using a third-party quantitative assessment as of the first day of the fourth quarter of fiscal years 2021, 2020year 2023. The fair value of each reporting unit was determined and 2019, respectively,compared to the carrying value. The inputs to the fair value are defined in the fair value hierarchy as Level 3 inputs. If the carrying value had exceeded the fair value, an impairment charge would have been recorded based on that difference. The annual impairment analysis resulted in no impairment for 2023. Management completed the annual impairment analysis of goodwill using a qualitative approach during fiscal year 2022, which resulted in no impairment charges.

The following table summarizes goodwill by reportable segment:

 

 

Food
Safety

 

 

Animal
Safety

 

 

Total

 

Balance, May 31, 2021

 

$

67,822

 

 

$

63,654

 

 

$

131,476

 

Acquisitions

 

 

4,152

 

 

 

11,752

 

 

 

15,904

 

Foreign currency translation and other

 

 

(4,416

)

 

 

(260

)

 

 

(4,676

)

Balance, May 31, 2022

 

$

67,558

 

 

$

75,146

 

 

$

142,704

 

Acquisitions (1)

 

 

1,985,476

 

 

 

6,783

 

 

 

1,992,259

 

Foreign currency translation and other

 

 

3,127

 

 

 

(594

)

 

 

2,533

 

Balance, May 31, 2023

 

$

2,056,161

 

 

$

81,335

 

 

$

2,137,496

 

(1) Animal Safety acquisitions represents portion of FSD transaction recorded at Neogen Australasia.

F-18


Other Intangible Assets

As of May 31, 2023, non-amortizable intangible assets included licenses of $569, trademarks of $12,522 and other intangibles of $1,224. During fiscal year 2023, the Company recorded an impairment of $1,000 to its non-amortizable trademarks related to discontinued product lines.

As of May 31, 2022, non-amortizable intangible assets included licenses of $569, trademarks of $13,604 and other intangibles of $1,224.

Management completed the annual impairment analysis of intangible assets with indefinite lives using a qualitative assessment for fiscal year 2023 and a quantitative assessment for fiscal year 2022. Other than the impairment in fiscal year 2023 related to the discrete trademarks discussed above, management determined that recorded amounts were not impaired and that no write-down wasimpairment charges were necessary.

The following table summarizes goodwill by reportable segment:
(in thousands)
  
Food Safety
   
Animal Safety
   
Total
 
Balance, May 31, 2019
  $ 42,553   $ 61,066   $ 103,619 
Goodwill acquired
   6,254    2,095    8,349 
Goodwill and/or currency adjustments (1)
   (1,592   (36   (1,628
                
Balance, May 31, 2020
  $47,215   $63,125   $110,340 
Goodwill acquired
   18,775    0    18,775 
Goodwill and/or currency adjustments (1)
   1,832    529    2,361 
                
Balance, May 31, 2021
  $67,822   $63,654   $131,476 
                
(1)
Includes final purchase price allocation adjustments and currency adjustments for goodwill recorded at international locations.
At May 31, 2021,
non-amortizable
intangible assets included licenses of $569,000, trademarks of $13,752,000 and other intangibles of $1,224,000. At May 31, 2020,
non-amortizable
intangible assets included licenses of $569,000, trademarks of $13,424,000 and other intangibles of $1,224,000.
F-20

Amortizable intangible assets consisted of the following and are included in customer-based intangibles and other

non-current
amortizable intangible assets within the consolidated balance sheets:

 

 

Gross
Carrying
Amount

 

 

Less
Accumulated
Amortization

 

 

Net
Carrying
Amount

 

Licenses

 

$

16,010

 

 

$

6,763

 

 

$

9,247

 

Covenants not to compete

 

 

488

 

 

 

384

 

 

 

104

 

Patents

 

 

8,499

 

 

 

4,865

 

 

 

3,634

 

Customer relationships intangibles

 

 

1,244,635

 

 

 

81,577

 

 

 

1,163,058

 

Trade names and trademarks

 

 

111,172

 

 

 

3,583

 

 

 

107,589

 

Developed technology

 

 

309,609

 

 

 

20,175

 

 

 

289,434

 

Other product and service-related intangibles

 

 

23,628

 

 

 

5,907

 

 

 

17,721

 

Balance, May 31, 2023

 

$

1,714,041

 

 

$

123,254

 

 

$

1,590,787

 

 

 

 

 

 

 

 

 

 

 

Licenses

 

$

17,109

 

 

$

5,682

 

 

$

11,427

 

Covenants not to compete

 

 

846

 

 

 

671

 

 

 

175

 

Patents

 

 

8,347

 

 

 

4,583

 

 

 

3,764

 

Customer relationships intangibles

 

 

75,000

 

 

 

33,662

 

 

 

41,338

 

Trade names and trademarks

 

 

1,180

 

 

 

167

 

 

 

1,013

 

Developed technology

 

 

17,741

 

 

 

6,124

 

 

 

11,617

 

Other product and service-related intangibles

 

 

27,299

 

 

 

4,527

 

 

 

22,772

 

Balance, May 31, 2022

 

$

147,522

 

 

$

55,416

 

 

$

92,106

 

(in thousands)
  
Gross
Carrying
Amount
   
Less
Accumulated
Amortization
   
Net
Carrying
Amount
 
Licenses
  $16,913   $4,580   $12,333 
Covenants not to compete
   1,006    571    435 
Patents
   8,363    4,243    4,120 
Customer-based intangibles
   76,384    35,209    41,175 
Other products and service-related intangibles
   27,567    8,859    18,708 
                
Balance, May 31, 2021
  $130,233   $53,462   $76,771 
                
             
Licenses
  $ 10,346   $3,330   $7,016 
Covenants not to compete
   706    407    299 
Patents
   8,509    4,118    4,391 
Customer-based intangibles
   59,847    29,898    29,949 
Other products and service-related intangibles
   16,646    6,937    9,709 
                
Balance, May 31, 2020
  $96,054   $ 44,690   $ 51,364 
                

During fiscal year 2023, the Company recorded an impairment of $2,109 to its amortizable licenses related to discontinued product lines.

Amortization expense for intangibles totaled $7,753,000, $6,489,000$71,085, $9,600, and $6,309,000$7,753 in fiscal years 2021, 2020,2023, 2022, and 2019,2021, respectively. The estimated amortization expense for each of the five succeeding fiscal years is as follows: $8,331,000 in 2022, $7,639,000 in 2023, $7,335,000$93,200 in 2024, $7,007,000$92,900 in 2025, $92,300 in 2026, $91,700 in 2027, $90,900 in 2028 and $6,943,000 in 2026. $1,129,987 thereafter.

The amortizable intangible assetsassets' useful lives are 2 to 20 years for licenses, 23 to 1310 years for covenants not to compete, 5 to 25 years for patents, 59 to 20 years for customer-based intangiblescustomer relationships, 10 to 25 years for trade names and 5trademarks, 10 to 20 years for developed technology and 5 to 15 years for other product and service-related intangibles, which primarily consist of product formulations.intangibles. All definite-lived intangibles are amortized on a straight-line basis with the exception of definite-lived customer-basedcustomer relationships intangibles and product and service-related intangibles, which are amortized on either a straight-line or an accelerated basis.

The weighted average remaining amortization period for intangibles was 18 years as of May 31, 2023 and eight years as of May 31, 2022.

F-19


3.
Business Combinations
3.
Business Combinations

The Consolidated Statements of Income (Loss) reflect the results of operations for business acquisitions since the respective dates of purchase. All are accounted for using the acquisition method. Goodwill recognized in the acquisitions described below relates primarily to enhancing the Company’s strategic platform for the expansion of available product offerings.

Fiscal 2019
On August 1, 2018, the Company acquired all of the stock of Clarus Labs, Inc., a manufacturer of water testing products. Neogen has distributed Clarus’ Colitag water test to the food and beverage industries since 2004; this acquisition has given the Company the ability to sell this product to new markets. Consideration for the purchase was $4,204,000 in cash and $1,256,000 of contingent consideration, due semiannually for the first five years, based on an excess net sales formula. The final purchase price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included inventory of $32,000, machinery and equipment of $120,000, accounts payable of $53,000, contingent consideration accrual of $1,256,000,
non-current
deferred tax liability of $544,000,
non-amortizable
intangible assets of $878,000, intangible assets of $1,487,000 (with an estimated life of
5-15
years) and the remainder to goodwill
(non-deductible
for tax purposes). These values are Level 3 fair value measurements. Since February 2019, $450,000 has been paid to the former owners as contingent consideration from the accrual. Manufacturing of these products was moved to the Company’s Lansing, Michigan location in October 2018, reporting within the Food Safety segment
.
On September 4, 2018, the Company acquired the assets of Livestock Genetic Services, LLC, a Virginia-based company that specializes in genetic evaluations and data management for cattle breeding organizations. Livestock Genetic Services had been a long-time strategic partner of Neogen and the acquisition enhanced the Company’s
in-house
genetic evaluation capabilities. Consideration for the purchase was $1,100,000 in cash, with $700,000 paid at closing and $400,000 payable to the former owner on September 1, 2019, and up to $585,000 of contingent consideration, payable over the next three years. The final purchase price allocation, based upon the fair value of these assets and
liabilities determined using the income approach, included office equipment of $15,000, contingent consideration accrual of $385,000, intangible assets of $942,000 (with an estimated life of
5-15
years) and the remainder to goodwill (deductible for tax purposes). These values are Level 3 fair value measurements. In September 2019, the former owner was paid the $400,000 installment of the purchase price owed and was also paid $107,000
in contingent consideration based on the achievement of sales targets in the first year. In November 2020, the former owner was paid $100,000 in contingent consideration based on the achievement of sales targets in the second year; the accrual was adjusted to the expected payment for the final year and, as a result, $37,000 was recorded as a gain in Other Income. Services provided by this operation are now performed at the Company’s Lincoln, Nebraska location, reporting within the Animal Safety segment.
F-21

On January 1, 2019, the Company acquired the assets of Edmonton, Alberta based Delta Genomics Centre, an animal genomics laboratory in Canada. Delta’s laboratory operations were renamed Neogen Canada and the acquisition was intended to accelerate growth of the Company’s animal genomics business in Canada. Consideration for the purchase was $1,485,000 in cash. The final purchase price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included inventory of $38,000, machinery and equipment of $371,000, unearned revenue liability of $125,000, intangible assets of $532,000 (with an estimated life of 5 to 10 years) and the remainder to goodwill (deductible for tax purposes). These values are Level 3 fair value measurements. Services provided by this operation continue to be performed in Edmonton, reporting within the Animal Safety segment.
Fiscal 2020
On January 1, 2020, the Company acquired all of the stock of Productos Quimicos Magiar, a distributor of Neogen’s Food Safety products for the past 20 years, located in Argentina. This acquisition gives Neogen a direct sales presence in Argentina. Consideration for the purchase was $3,776,000 in net cash, with $3,237,000 paid at closing and $540,000 payable to the former owner on January 1, 2022, and up to $979,000 of contingent consideration, payable in one year, based upon an excess net sales formula.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $603,000, inventory of $446,000, machinery and equipment of $36,000, other current assets of $221,000, accounts payable of $383,000, other current liabilities of $312,000, contingent consideration accrual of $640,000,
non-current
deferred tax liabilities of $441,000, intangible assets of $1,471,000 (with an estimated life of
5-10
years)
and the remainder to goodwill
(non-deductible
for tax purposes). These values are Level 3 fair value measurements. In February 2021, the former owner was paid $530,000 of contingent consideration based on the achievement of sales targets; the remaining $110,000 accrued but not earned was recorded as a gain in Other Income in the third quarter of fiscal 2021. This operation continues to operate from its current location in Buenos Aires, Argentina, reporting within the Food Safety segment. It is managed through Neogen’s Latin America operation.
On January 1, 2020, the Company acquired all of the stock of Productos Quimicos Magiar, a distributor of Neogen’s Food Safety products for the past 20 years, located in Uruguay. This acquisition gives Neogen a direct sales presence in Uruguay. Consideration for the purchase was $1,488,000 in net cash, with $1,278,000 paid at closing and $210,000 payable to the former owner on January 1, 2022, and up to $241,000 in contingent consideration, payable in one year, based upon an excess net sales formula.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $280,000, inventory of $174,000, machinery and equipment of $16,000, other current assets of $68,000, accounts payable of $204,000, other current liabilities of $11,000, contingent consideration accrual of $159,000,
non-current
deferred tax liabilities of $99,000, intangible assets of $398,000 (with an estimated life of
5-10
years) and the remainder to goodwill
(non-deductible for tax purposes). These values are Level 3 fair value measurements. In February 2021, the former owner was paid $158,000 of contingent consideration based on the achievement of sales targets; the remaining $1,000 accrued but not earned was recorded as a gain in Other Income in the third quarter of fiscal 2021. This operation continues to operate from its current location in Montevideo, Uruguay, reporting within the Food Safety segment. It is managed through Neogen’s Latin America operation.
On January 9, 2020, the Company acquired all of the stock of Diessechem Srl, a distributor of food and feed diagnostics for the past 27 years, located in Italy. This acquisition gives Neogen a direct sales presence in Italy. Consideration for the purchase was $3,455,000 in net cash.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $780,000, inventory of $5,000, other current assets of $160,000, accounts payable of $140,000, other current liabilities of $305,000,
non-current
deferred tax liabilities of $294,000, intangible assets of $1,225,000 (with an estimated life of
5-10
years) and the remainder to goodwill
(non-deductible
for tax purposes). These values are Level 3 fair value measurements. This operation continues to operate from its current location in Milan, Italy, reporting within the Food Safety segment. It is managed through Neogen’s Scotland operation.
F-22

On January 31, 2020, the Company acquired all of the stock of Abtek Biologicals Limited, a manufacturer and supplier of culture media supplements and microbiology technologies. This acquisition enhances the Company’s culture media product line offering for the worldwide industrial microbiology markets. Consideration for the purchase was $1,401,000 in net cash, with $1,282,000 paid at closing and $119,000 payable to the former owner on January 31, 2021.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $135,000, inventory of $207,000, machinery and equipment of $105,000, prepayments of $6,000, accounts payable of $118,000, other current liabilities of $34,000,
non-current
deferred tax liabilities of $92,000, intangible assets of $484,000 (with an estimated life of
5-10
years) and the remainder to goodwill
(non-deductible
for tax purposes). These values are Level 3 fair value measurements.
The final $119,000 owed was paid to the former owner in January 2021. This manufacturing operation continues to operate from its current location in Liverpool, England, reporting within the Food Safety segment. It is managed through Neogen’s Scotland operation. 
On February 28, 2020, the Company acquired the assets of Cell BioSciences, an Australian distributor of food safety and industrial microbiology products. This acquisition
gives
Neogen a direct sales presence across Australasia for its entire product portfolio. Consideration for the purchase was $3,768,000 in cash, with $3,596,000 paid at closing and $172,000 payable in one year.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included inventory of $420,000, unearned revenue liability of $13,000, intangible assets of $1,338,000 (with an estimated life of 3 to 10 years)
and the remainder to goodwill (non-deductible for tax purposes). These values are Level 3 fair value measurements. The final $172,000 owed was paid to the former owner in March 2021. The business operates in Gatton, Australia, reporting within the Australian operations in the Animal Safety segment. 
On March 26, 2020, the Company acquired the assets of Chile-based Magiar Chilena, a distributor of food, animal and plant diagnostics, including Neogen products. This acquisition gives Neogen a direct sales presence in Chile. Consideration for the purchase was $400,000 in cash, with $350,000 paid at closing and $50,000 payable to the former owner on March 26, 2021.
The final purchase 
price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included inventory of $164,000, machinery and equipment of $53,000, and intangible assets of $183,000 (with an estimated life of
5-10
years). The business is operated from its current location in Santiago, Chile, reporting within the Food Safety segment. It is managed through Neogen’s Latin America operation.

Fiscal 2021

On

In July 31, 2020, the Company acquired the U.S. (including territories) rights to Elanco’s StandGuard

Pour-on
for horn fly and lice control in beef cattle, and related assets. This product line fits in well with Neogen’s existing agricultural insecticide portfolio and organizational capabilities. Consideration for the purchase was $2,351,000$2,351 in cash, all paid at closing.
The final purchase
price allocation, based upon the fair value of these assets determined using the income approach, included inventory of $51,000$
51 and intangible assets of $2,300,000 (with an estimated life of 15 years)$2,300. This product line is currently being toll manufactured for the Company but is eventually expected to be manufactured at Neogen’s operation in Iowa; the salesSales are reported within the Animal Safety segment.
On

In December 30, 2020, the Company acquired all of the stock of Megazyme, Ltd, an Ireland-based company, and its wholly-owned subsidiaries, U.S.-based Megazyme, Inc. and Ireland-based Megazyme IP. Megazyme is a manufacturer and supplier of diagnostic assay kits and enzymes to measure dietary fiber, complex carbohydrates and enzymes in food and beverages as well as animal feeds. This acquisition will allow Neogen to expand its commercial relationships across food, feed and beverage companies, and provide additional food quality diagnostic products to commercial labs and food science research institutions. Consideration for the purchase was net cash of

$39.8 million39,800 paid at closing, $8.6 
million$8,600 of cash placed in escrow payable to the former owner in two installments in two and four years,
$4.9 million
4,900 of stock issued at closing, and up to $2.5 million$2,500 of contingent consideration, payable in two installments over the next year, based upon an excess net sales formula. The preliminaryfinal purchase price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $1,376,000,$1,376, inventory of $5,595,000,$5,595, net property, plant and equipment of $12,599,000,$12,599, prepayments of $69,000, accounts payable of $4,000,$69, other current liabilities of $1,815,000,$1,815, contingent consideration accrual of $2,458,000,
$2,458, non-current liabilities of $319,000,$319, non-current
deferred tax liabilities of $3,306,000,$
3,306, intangible assets of $22,945,000 (with an estimated life of
15-20
years)$
22,945 and the remainder to goodwill
(non-deductible
(non-deductible for tax purposes). These values are Level 3 fair value measurements. In February 2021,the year subsequent to the acquisition, payments of $
2,349 were made to the former owner was paid $1,229,000 forowner. In the second year after the acquisition, the first escrow installment of contingent consideration, based upon the achievement of sales targets.
payment was also made. The Irish companies continue to operate from their current locations in Bray, Ireland, reporting within the Food Safety segment and are managed through Neogen’s Scotland operation. The Company’s U.S. company’s business is now managed by our Lansing-based Food Safety team.

Fiscal 2022

In September 2021, the Company acquired all of the stock of CAPInnoVet, Inc., a companion animal health business that provides pet medications to the veterinary market. This acquisition provided entry into the retail parasiticide market and enhanced the Company’s presence in companion animal markets. Consideration for the purchase was net cash of $17,900 paid at closing. There also is the potential for performance milestone payments to the former owners of up to $6,500 and the Company could incur up to $14,500 in future royalty payments. The final purchase allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $308, inventory of $531, prepayments of $296, accounts payable of $120, other current liabilities of $84, non-current liabilities of $6,500, intangible assets of $19,200 and the remainder to goodwill (deductible for tax purposes). Upon revaluation of the contingent liability during the third quarter of fiscal year 2023, the Company recognized a gain of $300 on the performance milestone liability, recorded within other income. The business is operated from our location in Lexington, KY, reporting within the Animal Safety segment.

In November 2021, the Company acquired all of the stock of Delf (U.K.) Ltd., a United Kingdom-based manufacturer and supplier of animal hygiene and industrial cleaning products, and Abbott Analytical Ltd., a related service provider. This acquisition expanded the Company’s line of dairy hygiene products and enhances our cleaner and disinfectant product portfolio. Consideration for the purchase was net cash of $9,500 paid at closing. The final purchase price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included accounts receivable of $1,059, inventory of $972, net property, plant and equipment of $152, prepayments of $31, accounts payable of $497, other current liabilities of $378, non-current deferred tax liabilities of $780, intangible assets of $3,100 and the remainder to goodwill (non-deductible for tax purposes). The companies continue to operate from their current location in Liverpool, England, reporting within the Food Safety segment and are managed through Neogen’s Scotland operation.

In December 2021, the Company acquired all of the stock of Genetic Veterinary Sciences, Inc., a companion animal genetic testing business providing genetic information for dogs, cats and birds to animal owners, breeders and veterinarians. This acquisition further will expand the Company’s presence in the companion animal market. Consideration for the purchase was $11,300 in net cash. The final purchase price allocation, based upon the fair value of these assets and liabilities

F-20


determined using the income approach, included accounts receivable of $38, net inventory of $292, net property, plant and equipment of $399, prepayments of $54, accounts payable of $325, unearned revenue of $1,900, other current liabilities of $321, intangible assets of $5,500 and the remainder to goodwill (deductible for tax purposes). The business is operated from its current location in Spokane, Washington, reporting within the Animal Safety segment. Since completion of initial estimates in the second quarter of fiscal year 2022, the Company has recorded insignificant measurement period adjustments, which resulted in a decrease to the base purchase price.

Fiscal 2023

Thai-Neo Biotech Co., Ltd. Acquisition

On July 1, 2022, the Company acquired all of the stock of Thai-Neo Biotech Co., Ltd., a longstanding distributor of Neogen’s food safety products to Thailand and Southeast Asia. This acquisition gives Neogen a direct sales presence in Thailand. Consideration for the purchase was $1,581 in net cash, with $1,310 paid at closing, $37 paid on November 29, 2022 as a working capital adjustment and $234 payable on October 1, 2023. The final purchase price allocation, based upon the fair value of these assets and liabilities determined using the income approach, included intangible assets of $620 (with an estimated life of 10 years). The business continues to operate in Bangkok, Thailand, reporting within the Food Safety segment.

Corvium Acquisition

On February 10, 2023, the Company acquired certain assets as part of an asset purchase agreement with Corvium, Inc., a partner and supplier within the Company's software analytics platform. This acquisition, which primarily includes the software technology, advances the Company's food safety data analytics strategy. The purchase price consideration was $24,067, which included $9,004 held in escrow. Subsequent to May 31, 2023, $8,000 of the escrow balance was released to Corvium, Inc. in July 2023. This transaction is a business combination and was accounted for using the acquisition method.

There also is the potential for performance milestone payments of up to $8,500 based on successful implementation of the software service at customer sites and sale of licenses. As a result, the Company has recorded contingent liabilities of $930 as part of the opening balance sheet within Other non-current liabilities, as shown below.

In the fourth quarter of fiscal 2023, the Company recorded adjustments to intangible assets of $3,820 and contingent liability of $1,070, which decreased the balances, based on a third-party advisor's valuation work and fair value estimates. Goodwill, which is fully deductible for tax purposes, includes value associated with profits earned from data management solutions that can be offered to existing customers and the expertise and reputation of the assembled workforce. These values are Level 3 fair value measurements.

Our estimates and assumptions are subject to change within the measurement period (up to one year from the acquisition date). While we believe that these preliminary estimates provide a reasonable basis for estimating the fair value of the assets acquired and liabilities assumed, we will continue to evaluate available information prior to finalization of the amounts. The primary areas of the preliminary purchase price allocation that are not yet finalized relate to the fair value of intangible assets.

Due to the Company's acquisition of Corvium, Inc., it recorded a loss of $1,500 during fiscal year 2023 on dissolution of its minority interest in that company.

The following table summarizes the preliminary fair value of assets acquired and liabilities assumed as of the date of acquisition:

F-21


Prepaids and other current assets

 

$

66

 

Property, plant and equipment

 

 

13

 

Intangible assets

 

 

10,180

 

Deferred revenue

 

 

(1,827

)

Adjustment of annual license prepaid

 

 

(419

)

Other non-current liabilities

 

 

(930

)

Total identifiable assets and liabilities acquired

 

 

7,083

 

Goodwill

 

 

16,984

 

Total purchase consideration

 

$

24,067

 

For each completed acquisition listed above, the revenues and net income were not considered material and were therefore not disclosed.

F-23

Table

3M Food Safety transaction

On September 1, 2022, Neogen, 3M Company (“3M”), and Neogen Food Safety Corporation (“Neogen Food Safety Corporation”), a subsidiary created to carve out 3M’s Food Safety Division (“3M FSD”, “FSD”), closed on the transaction combining 3M’s FSD with Neogen in a Reverse Morris Trust transaction and Neogen Food Safety Corporation became a wholly owned subsidiary of ContentsNeogen (“FSD transaction”). Immediately following the FSD transaction, pre-merger Neogen Food Safety Corporation stockholders owned, in the aggregate, approximately 50.1% of the issued and outstanding shares of Neogen common stock and pre-merger Neogen shareholders owned, in the aggregate, approximately 49.9% of the issued and outstanding shares of Neogen common stock. This transaction is a business combination and was accounted for using the acquisition method.

The acquired business is a leading provider of food safety testing solutions. It offers a broad range of food safety testing products that support multiple industries within food and beverage, helping producers to prevent and protect consumers from foodborne illnesses. The business has a broad global presence with products used in more than 60 countries and a diversified revenue base of more than 100,000 end-user customers. The combination of Neogen and the 3M FSD creates a leading innovator with an enhanced geographic footprint, innovative product offerings, digitization capabilities, and financial flexibility to capitalize on robust growth trends in sustainability, food safety, and supply chain integrity. The acquired Food Safety business continues to primarily operate in facilities in Minnesota and the United Kingdom ("U.K."), and is being managed overall in Michigan, reporting within the Food Safety segment.

The purchase price consideration for the 3M FSD was $3.2 billion, net of customary purchase price adjustments and transaction costs, which consisted of 108,269,946 shares of Neogen common stock issued on closing with a fair value of $2.2 billion and cash consideration of $1 billion, funded by the additional financing secured by the Company. See Note 4 "Long-Term Debt" for further detail on the debt incurred.

During the fiscal year ended May 31, 2023, the Company recorded adjustments to its preliminary allocation of the purchase consideration to assets acquired and liabilities assumed based on initial fair value estimates and is subject to continuing management analysis, with assistance from third-party valuation advisors. In the fourth quarter of fiscal 2023, Inventory and Property, plant and equipment amounts were finalized. The excess of the purchase price over the fair value of the net tangible assets and identifiable intangible assets of $1.97 billion was recorded as goodwill, of which $1.92 billion is non-deductible for tax purposes. Goodwill includes value associated with profits earned from market and expansion capabilities, expected synergies from integration and streamlining operational activities, the expertise and reputation of the assembled workforce and other intangible assets that do not qualify for separate recognition. These values are Level 3 fair value measurements.

The preliminary fair values of net tangible assets and intangible assets acquired were based on preliminary valuations, and our estimates and assumptions are subject to change within the measurement period (up to one year from the acquisition date). The primary areas of the preliminary purchase price allocation that are not yet finalized relate to deferred income tax liabilities. The fair values of the assets acquired and liabilities assumed are based on our preliminary estimates and assumptions, as well as other information compiled by management, including valuations that utilize customary valuation procedures and techniques. While we believe that these preliminary estimates provide a reasonable basis for estimating the

F-22


fair value of the assets acquired and liabilities assumed, we will continue to evaluate available information prior to finalization of the amounts.

The following table summarizes the preliminary fair value of assets acquired and liabilities assumed as of the date of acquisition:

 

 

 

 

Cash and cash equivalents

 

$

319

 

Inventories

 

 

18,403

 

Other current assets

 

 

14,855

 

Property, plant and equipment

 

 

25,832

 

Intangible assets

 

 

1,560,000

 

Right of use asset

 

 

882

 

Lease liability

 

 

(885

)

Deferred tax liabilities

 

 

(352,481

)

Other liabilities

 

 

(2,832

)

Total identifiable assets and liabilities acquired

 

 

1,264,093

 

Goodwill

 

 

1,974,520

 

Total purchase consideration

 

$

3,238,613

 

The following table summarizes the intangible assets acquired and the useful life of these assets.

 

 

Fair Value

 

 

Useful Life in Years

 

Trade Names and Trademarks

 

$

110,000

 

 

 

25

 

Developed Technology

 

 

280,000

 

 

 

15

 

Customer Relationships

 

 

1,170,000

 

 

 

20

 

Total intangible assets acquired

 

$

1,560,000

 

 

 

 

4.
Long-Term Debt

The Company hasdetermined the fair value of the acquired customer relationships intangible assets by applying the multi-period excess earnings method, which involved the use of significant estimates and assumptions related to forecasted revenue growth rate and customer attrition rate. Valuation specialists were used to develop and evaluate the appropriateness of the multi-period excess earnings method, the Company's discount rates, attrition rate and fair value estimates using its cash flow projections.

During the twelve months ended May 31, 2023, transaction fees and integration costs of $58,175 were expensed. In the twelve months ended May 31, 2022, acquisition related costs of $25,581 were expensed. These costs are included in general and administrative expenses in the Company’s consolidated statements of income (loss).

The operating results of the FSD have been included in the Company’s consolidated statements of income (loss) since the acquisition date. In fiscal year 2023, the FSD’s total revenue was $279,541 and operating loss was approximately $28,200. The operating loss includes $58,175 of transaction fees and integration expenses, $60,872 of amortization expense for acquired intangible assets and a $3,245 charge to cost of goods sold related to the step up to fair value on acquired inventory.

The following table presents unaudited pro forma information as if the merger with the 3M FSD business had occurred on June 1, 2021 and had been combined with the results reported in our consolidated statements of income (loss) for all periods presented:

 

Year Ended May 31

 

 

 

2023

 

 

2022

 

Net sales

 

$

919,959

 

 

$

910,978

 

Operating income

 

$

44,373

 

 

$

42,258

 

The unaudited pro forma information is presented for informational purposes only and is not indicative of the results that would have been achieved if the merger had taken place at such time. The unaudited pro forma information presented

F-23


above includes adjustments primarily for amortization charges for acquired intangible assets and certain acquisition-related expenses for legal and professional fees.

In connection with the acquisition of the 3M FSD, the Company and 3M entered into several transition service agreements, including manufacturing, distribution and certain back-office support, that have been accounted for separately from the acquisition of assets and assumption of liabilities in the business combination. 3M periodically remits amounts charged to customers on our behalf and charges us for the associated cost of goods sold and transition service fees. Additionally, 3M is reimbursing the Company for a portion of its SAP implementation costs. As of May 31, 2023, a receivable from 3M of $12,365 was included in prepaid expenses and other current assets in the Company’s consolidated balance sheets.

4.
Long-Term Debt

The Company’s long-term debt consists of the following:

 

 

May 31, 2023

 

Term Loan

 

$

550,000

 

Senior Notes

 

 

350,000

 

Total long-term debt

 

 

900,000

 

Less: Unamortized debt issuance costs

 

 

(14,561

)

Total non-current debt, net

 

$

885,439

 

The Company had a financing agreement with a bank providing for a

$15,000,000
15,000unsecured revolving line of credit, which was amended in the second quarter to extend the expiration to
originally expired on November 30, 2023.2023, but was replaced by the five-year senior secured revolving facility as part of the Credit Facilities described below. There were 0no advances against the line of credit during fiscal years 20212022 and 2020; there were no advances in fiscal 2023 before the line of credit was 0 balance outstanding at May 31, 2021.extinguished. Interest on any borrowings is
under that agreement was at
LIBOR plus 100 basis points (rate under the terms of the agreement was 1.06%
at May 31, 2021). See Note 1, Recent Accounting Pronouncements Not Yet Adopted, for information on reference rate reform. Financial covenants includeincluded maintaining specified levels of tangible net worth, debt service coverage, and funded debt to EBITDA;EBITDA, each of which the Company believes it was in compliance with these covenants atduring the period the line of credit was available.

As of May 31, 2021. 2022, the Company had no outstanding debt. In connection with the acquisition of 3M’s Food Safety business as described more fully in Note 8, Neogen incurred financing through Neogen Food Safety Corporation as follows:

Credit Facilities

On June 30, 2022, Neogen Food Safety Corporation entered into a credit agreement consisting of a five-year senior secured term loan facility (“term loan facility”) in the amount of $650,000 and a five-year senior secured revolving facility (“revolving facility”) in the amount of $150,000 (collectively, the “Credit Facilities”) to fund the FSD transaction. The term loan facility was drawn on August 31, 2022, to fund the closing of the FSD transaction on September 1, 2022 while the revolving facility was undrawn and continues to be undrawn as of May 31, 2023.

The Credit Facilities bear interest based on term SOFR plus an applicable margin which ranges between 150 to 225 basis points, determined for each interest period and paid monthly. During the twelve months ended May 31, 2023, the interest rates ranged from 4.81% to 7.33% per annum. The term loan facility matures on June 30, 2027 and the revolving facility matures at the earlier of June 30, 2027 and the termination of the revolving commitments. The Company paid $60,000 of the term loan facility’s principal in September 2022 and an additional $40,000 of the term loan facility's principal in December 2022, in order to decrease the outstanding debt balance.

The term loan facility contains an optional prepayment feature at the discretion of the Company. The Company determined that the prepayment feature did not meet the definition of an embedded derivative and does not require bifurcation from the host liability and, accordingly, has accounted for the entire instrument at amortized cost.

F-24


In November 2022, the Company entered into an interest rate swap agreement, whereby interest on $250,000 of the total $550,000 principal balance is paid at a fixed rate. See Note 9. "Fair Value and Derivatives" for further detail on the interest rate swap agreement.

The Company can draw any amount under the revolving facility up to the $150,000 limit, with the amount to be repaid on the termination date of the revolving commitments. Debt issuance costs of $2,361 were incurred related to the revolving facility. These costs are being amortized as interest expense in the consolidated statements of (loss) income over the contractual life of the revolving facility using the straight line method. Amortization of the deferred debt issuance costs for the revolving facility was $366 during the twelve months ended May 31, 2023. Debt issuance costs of $489 were recorded in Prepaid expenses and other current assets and $1,506 were recorded in Other non-current assets on the consolidated balance sheet as of May 31, 2023. The Company must pay an annual commitment fee ranging from 0.20% and 0.35% on the unused portion of the Revolving Credit Facility, paid quarterly. As of May 31, 2023, the commitment fee was 0.35% and $473 was recorded as interest expense in the consolidated statements of income (loss) during the twelve months ended May 31, 2023.

Accrued interest payable on the term loan as of May 31, 2023 was $164. The Company incurred $10,232 in total debt issuance costs on the term loan which is recorded as an offset to the term loan facility and amortized over the contractual life of the loan to interest expense using the straight line method. The amortization of deferred debt issuance costs of $1,588 and interest expense of $27,254 (excluding swap credit of $577) for the term loan was included in the consolidated statements of income (loss) during the twelve months ended May 31, 2023.

Financial covenants include maintaining specified levels of funded debt to EBITDA, and debt service coverage. As of May 31, 2023, the Company was in compliance with its debt covenants.

Senior Notes

On July 20, 2022, Neogen Food Safety Corporation closed on an offering of $350,000 aggregate principal amount of 8.625% senior notes due 2030 (the “Notes”) in a private placement at par. The Notes were initially issued by Neogen Food Safety Corporation to 3M and were transferred and delivered by 3M to the selling securityholder in the offering, in satisfaction of certain of 3M’s existing debt. Upon closing of the FSD transaction on September 1, 2022, the Notes became guaranteed on a senior unsecured basis by the Company and certain wholly-owned domestic subsidiaries of the Company.

The Company determined that the redemption features of the Notes did not meet the definition of a derivative and thus does not require bifurcation from the host liability and accordingly has accounted for the entire instrument at amortized cost.

Total accrued interest on the Notes was $10,985 as of May 31, 2023 based on the stated interest rate of 8.625%. This amount was included in current liabilities on the consolidated balance sheets. The Company incurred total debt issuance costs of $6,683, which is recorded as an offset to the Notes and amortized over the contractual life of the Notes to interest expense using the straight line method. The amortization of deferred debt issuance costs of $766 and interest expense of $26,079 for the Notes was included in the consolidated statements of income (loss) during the twelve months ended May 31, 2023.

There are no required principal payments on the Term Loan or the Senior Notes through fiscal year 2026, due to $100,000 in prepayments made on the Term Loan in fiscal 2023. The expected maturities associated with the Company’s outstanding debt as of May 31, 2023, were as follows:

 

 

Amount

 

Fiscal Year

 

 

 

2024

 

$

 

2025

 

 

 

2026

 

 

 

2027

 

 

34,063

 

2028

 

 

515,937

 

Thereafter

 

 

350,000

 

Total

 

$

900,000

 

F-25


5.
Equity Compensation Plans
5.
Equity Compensation Plans

The Company’s long-term incentive plans allow for the grant of various types of share-based awards to officers, directors and other key employees of the Company. Incentive and

non-qualified
options to purchase shares of common stock have been granted to directors, officers and employees of Neogen under the terms of the Company’s stock option plans.2018 Omnibus Incentive Plan. These options wereare granted at an exercise price of not less than the fair market valueclosing price of the common stock on the date of grant. Remaining shares available for grant under stock option plans were 6,355,000, 7,002,000
and 7,994,000 at May 31, 2021, 2020 and 2019, respectively. Options vest ratably overthree threeand andfive year-year periods and the contractual terms are generally five, seven or ten years.years. The Company grants restricted stock units (RSUs) under the terms of the 2018 Omnibus Incentive Plan, which vest ratably over three and five year periods. The fair value of the options was estimated at the date of the grant using the Black-Scholes option pricing model. The fair value of the RSUs is determined based on the closing price of the common stock on the date of grant.

Remaining shares available for grant under share-based compensation plans were 2,871,000, 5,386,000, and 6,355,000 at May 31, 2023, 2022, and 2021, respectively. Compensation expense related to share-based awards was $10,177, $7,154, and $6,437 in fiscal years 2023, 2022, and 2021, respectively.

Options

 

 

 

 

 

 

 

 

 

(options in thousands)

 

Options

 

 

Weighted-Average Exercise Price

 

 

Weighted-Average Grant Date Fair Value

 

Outstanding at May 31, 2020 (972 exercisable)

 

 

4,324

 

 

$

27.98

 

 

$

6.98

 

Granted

 

 

403

 

 

 

34.23

 

 

 

7.71

 

Exercised

 

 

(1,389

)

 

 

24.38

 

 

 

6.31

 

Forfeited

 

 

(381

)

 

 

28.99

 

 

 

7.20

 

Outstanding at May 31, 2021 (643 exercisable)

 

 

2,957

 

 

 

27.98

 

 

 

6.98

 

Granted

 

 

615

 

 

 

36.42

 

 

 

8.49

 

Exercised

 

 

(281

)

 

 

22.79

 

 

 

6.29

 

Forfeited

 

 

(47

)

 

 

33.93

 

 

 

8.02

 

Outstanding at May 31, 2022 (1,191 exercisable)

 

 

3,244

 

 

 

32.13

 

 

 

7.66

 

Granted

 

 

1,704

 

 

 

14.68

 

 

 

4.61

 

Exercised

 

 

(22

)

 

 

14.78

 

 

 

4.23

 

Forfeited

 

 

(704

)

 

 

29.81

 

 

 

7.26

 

Outstanding at May 31, 2023 (1,401 exercisable)

 

 

4,222

 

 

 

25.56

 

 

 

6.51

 

(options in thousands)
  
Options
   
Weighted-Average

Exercise Price
   
Weighted-Average

Grant Date Fair Value
 
Outstanding at May 31, 2018 (1,016 exercisable)
   4,998   $  21.32   $  5.72 
Granted
   1,054    31.46    7.46 
Exercised
   (1,026)   15.64    4.46 
Forfeited
   (256)   23.54    6.21 
                
Outstanding at May 31, 2019 (1,234
 
exercisable)
   4,770    24.69    6.35 
Granted
   1,124    31.96    7.78 
Exercised
   (1,438)   20.12    5.53 
Forfeited
   (132)   28.72    7.10 
                
Outstanding at May 31, 2020 (972
 
exercisable)
   4,324    27.98    6.98 
Granted
   403    34.23      7.71   
Exercised
   (1,389)     24.38      6.31   
Forfeited
   (381)     28.99      7.20   
                
Outstanding at May 31, 2021 (643
 
exercisable)
   2,957    30.38      7.36   
                

The following is a summary of stock options outstanding at May 31, 2021:2023:

 

Options Outstanding

 

 

Options Exercisable

 

 

 

 

 

 

Average

 

 

 

 

 

 

 

 

 

 

(options in thousands)

 

 

 

 

Contractual Life

 

 

Weighted-Average

 

 

 

 

 

Weighted-Average

 

Range of Exercise Price

 

Number

 

 

(in years)

 

 

Exercise Price

 

 

Number

 

 

Exercise Price

 

$12.20 - $20.00

 

 

1,585

 

 

 

6.3

 

 

$

13.63

 

 

 

27

 

 

$

15.95

 

$20.01 - $28.00

 

 

138

 

 

 

6.7

 

 

 

25.11

 

 

 

90

 

 

 

23.93

 

$28.01 - $36.00

 

 

2,124

 

 

 

1.8

 

 

 

31.77

 

 

 

1,205

 

 

 

31.84

 

$36.01 - $42.15

 

 

375

 

 

 

3.4

 

 

 

40.94

 

 

 

79

 

 

 

40.99

 

 

 

 

4,222

 

 

 

3.8

 

 

$

25.56

 

 

 

1,401

 

 

$

31.54

 

   
Options Outstanding
   
Options Exercisable
 
       
Average
             
(options in thousands)
      
Contractual Life
   
Weighted-Average
       
Weighted-Average
 
Range of Exercise Price
  
Number
   
(in years)
   
Exercise Price
   
Number
   
Exercise Price
 
$10.75 - $20.00
   54    3.1   $15.65    51   $15.45 
$20.01 - $30.00
   376    1.8    22.55    150    23.07 
$30.01 - $31.50
   1,150    2.1    30.87    299    30.76 
$31.51 - $32.00
   898    3.4    31.95    101    31.95 
$32.01 - $35.28
   479    4.1    34.07    42    33.53 
                          
    2,957    2.8    30.38    643    28.10 

The weighted average exercise price of shares subject to options that were exercisable at May 31, 20202022 and 20192021 was

$24.4730.24 and $20.34,$28.10, respectively.

Compensation expense related to share-based awards was $6,437,000, $6,468,000 and $5,543,000 in fiscal years 2021, 2020 and 2019, respectively.

Remaining compensation cost to be expensed in future periods for

non-vested
options was $15,131,000$11,729 at May 31, 2021,2023, with a weighted average expense recognition period of 3.12.4 years.

F-26


 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Aggregate intrinsic value of options outstanding

 

$

6,154

 

 

$

850

 

 

$

46,667

 

Aggregate intrinsic value of options exercisable

 

$

42

 

 

$

817

 

 

$

11,617

 

Aggregate intrinsic value of options exercised

 

$

73

 

 

$

5,507

 

 

$

22,349

 

F-24

Table

The fair value of Contentsstock options granted was estimated using the following weighted-average assumptions:

 

Year ended May 31

 

 

2023

 

 

2022

 

 

2021

 

Risk-free interest rate

 

 

3.3

%

 

 

0.4

%

 

 

0.2

%

Expected dividend yield

 

 

0.0

%

 

 

0.0

%

 

 

0.0

%

Expected stock volatility

 

 

34.0

%

 

 

32.8

%

 

 

31.3

%

Expected option life

 

4.5 years

 

 

3.12 years

 

 

3.25 years

 

   
Year Ended
 
(in thousands)
  
May 31, 2021
   
May 31, 2020
   
May 31, 2019
 
Aggregate intrinsic value of options outstanding
  $46,667   $32,988   $22,798 
Aggregate intrinsic value of options exercisable
  $11,617   $10,814   $10,222 
Aggregate intrinsic value of options exerised
  $22,349   $19,597   $21,382 

The Companyrisk-free interest rate for periods within the expected life of options granted 118,250 restrictedis based on the United States Treasury yield curve in effect at the time of grant. Expected stock units (RSUs) to directors, officers and employees under the termsprice volatility is based on historical volatility of the 2018 Omnibus Incentive PlanCompany’s stock. The expected option life, representing the period of time that options granted are expected to be outstanding, is based on historical option exercise and employee termination data. We include recent historical experience in October 2020, which vest ratably over threeestimating our forfeitures. As employees terminate, grant tranches expire or as forfeitures are known, estimated expense is adjusted to actual. For options granted in fiscal years 2023, 2022, and five year periods. RSUs have a weighted average2021, the Company recorded charges in general and administrative expense based on the fair value of $34.21 per share and will bestock options using the straight-line method over the vesting period of three to five years.

Restricted Stock Units

The RSUs are expensed straight-line over the remaining weighted-average period of 4.242.7 years. On May 31, 20212023, there was $3,064,000$10,839 in unamortized compensation cost related to non-vested RSUs. The fair value of restricted stock units vested during fiscal years 2023 and 2022 was $820 and $1,032, respectively. There were no RSUs that vested during fiscal year 2021.

non-vested

(RSU Grants in thousands)

 

RSUs

 

 

Weighted Average Grant Date Fair Value

 

Outstanding at May 31, 2021

 

 

121

 

 

$

34.21

 

Granted

 

 

169

 

 

 

37.28

 

Released

 

 

(25

)

 

 

34.24

 

Forfeited

 

 

(8

)

 

 

36.80

 

Outstanding at May 31, 2022

 

 

257

 

 

 

36.14

 

Granted

 

 

596

 

 

 

13.83

 

Released

 

 

(60

)

 

 

35.14

 

Forfeited

 

 

(27

)

 

 

22.81

 

Outstanding at May 31, 2023

 

 

766

 

 

 

19.30

 

RSUs.

The weighted average grant date fair value of the fiscal year 2021 awards was $34.21.

Employee Stock Purchase Plan

The Company offers eligible employees the option to purchase common stock at a 5%5% discount to the lower of the market value of the stock at the beginning or end of each participation period under the terms of the 20112021 Employee Stock Purchase Plan; thePlan. The discount is recorded in general and administrative expense. Total individual purchases in any year are limited to 10%10% of compensation. Shares purchased by employees through this program were 38,406

94,604in fiscal 2021
, 43,156
2023, 43,456in fiscal 2020
2022, and
36,660
38,406in fiscal 2019.2021. As of May 31, 2021,2023, common stock totaling
 649,228881,323 of the 1,425,000
1,000,000authorized shares remained reserved for issuance under the plan.

F-27


6.
Income Taxes
6.
Income Taxes

Income before income taxes by source consists of the following amounts:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

U.S.

 

$

(85,681

)

 

$

38,554

 

 

$

55,753

 

Foreign

 

 

63,639

 

 

 

21,653

 

 

 

19,515

 

 

$

(22,042

)

 

$

60,207

 

 

$

75,268

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
   
2019
 
U.S.
  $    55,753   $62,329   $58,479 
Foreign
   19,515    9,976    14,480 
                
   $75,268   $72,305   $72,959 
                

The provision for income taxes consists of the following:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Current

 

 

 

 

 

 

 

 

 

Domestic

 

 

 

 

 

 

 

 

 

Federal

 

$

8,674

 

 

$

8,579

 

 

$

6,981

 

Change in tax-related uncertainties

 

 

278

 

 

 

3

 

 

 

(75

)

State

 

 

1,616

 

 

 

2,406

 

 

 

2,147

 

Foreign

 

 

9,490

 

 

 

5,140

 

 

 

4,875

 

Total Current

 

 

20,058

 

 

 

16,128

 

 

 

13,928

 

Deferred

 

 

 

 

 

 

 

 

 

Domestic

 

 

 

 

 

 

 

 

 

Federal

 

 

(17,406

)

 

 

(3,721

)

 

 

479

 

State

 

 

(1,865

)

 

 

(356

)

 

 

44

 

Foreign

 

 

41

 

 

 

(151

)

 

 

(65

)

Total Deferred

 

 

(19,230

)

 

 

(4,228

)

 

 

458

 

Provision for Income Taxes

 

$

828

 

 

$

11,900

 

 

$

14,386

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
   
2019
 
Current
 
              
Domestic
 
              
Federal
 
   $    6,981   $6,886   $7,173 
Change in tax-related uncertainties
 
  (75)     269    13 
State
 
  2,147    1,262    1,265 
Foreign
 
  4,875    2,475    3,758 
Deferred
 
              
Domestic
 
              
Federal
 
  479    1,964    1,031 
State
 
  44    195    98 
Foreign
 
  (65)     (221   (555
 
 
              
Provision for Income Taxes
 
  
 
 $
14,386   $12,830   $12,783 
 
 
              
F-25

The reconciliation of income taxes computed at the U.S. federal statutory tax rate to income tax expense is as follows:

 

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Tax at U.S. statutory rate

 

$

(4,629

)

 

$

12,643

 

 

$

15,806

 

Permanent differences

 

 

325

 

 

 

179

 

 

 

292

 

Global intangible low-taxed income (GILTI)

 

 

6,482

 

 

 

1,501

 

 

 

2,064

 

Foreign derived intangible income deduction (FDII)

 

 

(643

)

 

 

(1,308

)

 

 

(1,210

)

Foreign rate differential

 

 

(3,742

)

 

 

215

 

 

 

669

 

Subpart F income

 

 

152

 

 

 

397

 

 

 

628

 

Tax-effect from stock-based compensation

 

 

1,946

 

 

 

(462

)

 

 

(2,651

)

Provision for state income taxes, net of federal benefit

 

 

18

 

 

 

1,517

 

 

 

1,601

 

Non-deductible acquisition expenses

 

 

7,187

 

 

 

 

 

 

 

Tax credits

 

 

(6,709

)

 

 

(2,527

)

 

 

(3,298

)

Impact of tax rate changes

 

 

 

 

 

583

 

 

 

(75

)

Change in tax-related uncertainties

 

 

278

 

 

 

3

 

 

 

55

 

Changes in valuation allowances

 

 

355

 

 

 

85

 

 

 

 

Research expenditures deduction

 

 

(365

)

 

 

(112

)

 

 

 

Other

 

 

173

 

 

 

(814

)

 

 

505

 

Income Tax Expense

 

$

828

 

 

$

11,900

 

 

$

14,386

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
   
2019
 
Tax at U.S. statutory rate
  $15,806   $15,184   $15,321 
Permanent differences
   292    360    (56
Global intangible
low-taxed
income (GILTI)
   2,064    438    840 
Foreign derived intangible income deduction (FDII)
   (1,210)     (1,120   (1,531
Foreign rate differential
   669    (182   495 
Subpart F income
   628    634    842 
Tax benefits on stock-based compensation
   (2,651)     (1,998   (2,586
Changes in tax contingencies—Increase/(Release)
   (76)     269    13 
Provision for state income taxes, net of federal benefit
   1,601    1,412    1,251 
Tax Credits
   (3,298)     (1,417   (1,726
Other
   561    (750   (80
                
Tax Expense
  $14,386   $12,830   $12,783 
                

Foreign tax credits, primarily offsetting taxes associated with Subpart F and GILTI income, were $2,753,000, $945,000$5,324, $1,747, and $1,296,000$2,753 in fiscal years 2021, 20202023, 2022, and 2019,2021, respectively. The Company’s research and development credits were $545,000, $472,000$1,385, $780, and $430,000$545 in fiscal years 2023, 2022, and 2021, 2020 and 2019, respectively.

F-28


Deferred income taxes reflect the tax effects of temporary differences between the carrying amounts of assets and liabilities for financial reporting purposes and the amounts used for income tax purposes. Significant components of our deferred income tax liabilities and assets are as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

Deferred income tax liabilities

 

 

 

 

 

 

Indefinite and long-lived assets

 

$

(369,500

)

 

$

(22,709

)

Right of use asset

 

 

(1,834

)

 

 

(344

)

Prepaid expenses

 

 

(1,480

)

 

 

(884

)

 

 

(372,814

)

 

 

(23,937

)

Deferred income tax assets

 

 

 

 

 

 

Interest expense not currently deductible

 

 

5,782

 

 

 

 

Research and experimentation capitalization

 

 

5,868

 

 

 

 

Stock options

 

 

2,192

 

 

 

2,085

 

Inventories and accounts receivable

 

 

3,219

 

 

 

2,044

 

Tax loss carryforwards

 

 

3,909

 

 

 

561

 

Lease liability

 

 

1,899

 

 

 

382

 

Accrued expenses and other

 

 

1,981

 

 

 

2,422

 

 

 

24,850

 

 

 

7,494

 

Valuation allowance

 

 

(2,110

)

 

 

(568

)

Net deferred income tax liabilities

 

$

(350,074

)

 

$

(17,011

)

 

 

 

 

 

 

Net deferred income tax assets (jurisdictional)

 

$

3,353

 

 

$

575

 

Net deferred income tax liabilities (jurisdictional)

 

 

(353,427

)

 

 

(17,586

)

Net deferred income tax liabilities

 

$

(350,074

)

 

$

(17,011

)

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
 
Deferred income tax liabilities
          
Indefinite and long-lived assets
  $ (25,072)  $(20,867
Prepaid expense
s
   (721)     (795
           
    (25,793)     (21,662
Deferred income tax assets
          
Stock options
   1,106    1,479 
Inventories and accounts receivable
   2,081    1,336 
Tax loss carryforwards
   662    484 
Accrued expenses and other
   568    657 
Less: valuation allowances
   (541)   (419
           
    3,876    3,537 
           
Net deferred income tax liabilities
  $(21,917)    $(18,125
           
F-26

The Company has the following net operating loss carryforwards:

 

 

As of May 31, 2023

 

 

Expiry

U.S.

 

$

218

 

 

2037

Foreign

 

 

13,362

 

 

2024 to Indefinite

 

$

13,580

 

 

 

(in thousands)
  
As of
     
Jurisdiction
  
5/31/2021
   
Expiry
 
U.S.
  $345    2037 to indefinite 
Foreign
   1,938    2024 to 2039 
           
   $2,283      
           

Valuation allowances against certain deferred tax assets are established based on management’s determination of a more likely than not standard that the tax benefits will not be realized.

We are subject to income taxes in the U.S. (federal and state) and in numerous foreign jurisdictions. Significant judgment is required in evaluating our tax positions and determining our provision for income taxes. During the ordinary course of business, there are transactions and calculations for which the ultimate tax determination is uncertain. We establish reserves for

t
a
x-related
tax-related uncertainties based on estimates of whether, and the extent to which, additional taxes will be due. These reserves are established when we believe that certain positions might be challenged despite our belief that our tax return positions are fully supportable. We adjust these reserves in light of changing facts and circumsta
n
ces,circumstances, such as the outcome of tax audits. The provision for income taxes includes the impact of reserve provisions and changes to reserves that are considered appropriate.
The Company’s policy is to recognize both accrued interest expense and penalties related to unrecognized tax benefits in income tax expense. The amount of interest and penalties included in the unrecognized tax benefits reserve was $145 at May 31, 2023, $69 at May 31, 2022, and $65 at May 31, 2021. Of the total unrecognized tax benefits at May 31, 2023 and 2022, $1,087 and $808, respectively, comprise unrecognized tax positions that would, if recognized, affect our effective tax rate.

F-29


The reconciliation of our tax-related uncertaintiesunrecognized tax benefits is as follows:

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Beginning balance

 

$

741

 

 

$

764

 

 

$

762

 

Increase/(decrease) related to prior periods

 

 

2

 

 

 

(75

)

 

 

(182

)

Increase related to current period

 

 

479

 

 

 

147

 

 

 

184

 

Lapses of applicable statute of limitations

 

 

(276

)

 

 

(95

)

 

 

 

Ending balance

 

$

946

 

 

$

741

 

 

$

764

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
   
2019
 
Beginning balance
  $    880   $611   $598 
Increase/(decrease) related to prior periods
   (272)     56    (106
Increase
related
to current perio
d
   197    213    119 
                
Ending balance
  $805   $880   $611 
                

The Company is no longer subject to examination by the Internal Revenue Service for fiscal year 201

7
2019 and preceding years.

As of May 31, 2023, the Company has approximately $153 million of undistributed earnings in its foreign subsidiaries. Approximately $41 million of these earnings are no longer considered permanently reinvested. The incremental tax cost to repatriate these earnings to the US is immaterial. The Company has not provided deferred taxes on approximately $112 million of undistributed earnings from non-U.S. subsidiaries as of May 31, 2023 which are indefinitely reinvested in operations. Based on historical experience, as well as management’s future plans, earnings from these subsidiaries will continue to be re-invested indefinitely for future expansion and working capital needs. On an annual basis, we evaluate the current business environment and whether any new events or other external changes might require future evaluation of the decision to indefinitely re-invest these foreign earnings. It is not practical to determine the income tax liability that would be payable if such earnings were not reinvested indefinitely.

7.
Commitments and Contingencies
7.
Commitments and Contingencies

The Company is involved in environmental remediation and monitoring activities at its Randolph, Wisconsin manufacturing facility and accrues for related costs when such costs are determined to be probable and estimable. The Company currently utilizes a pump and treat remediation strategy, which includes semi-annual monitoring and reporting, consulting, and maintenance of monitoring wells. We expense these annual costs of remediation, which have ranged from $38,000$63 to $131,000 $131per year over the past five years. The Company’s estimated

remaining
liability for these costs was $916,000$916 at both May 31, 20212023 and 2020,2022, measured on an undiscounted basis over an estimated period of 15 years
.
years. In fiscal 2019, the Company performed an updated Corrective Measures Study on the site, per a request from the Wisconsin Department of Natural Resources (WDNR), and is currently in discussionworking with the WDNR regarding potential alternative remediation strategies going forward. The Company believes that the current pump and treat strategy is appropriate for the site. However, the Company has agreed toinitiated a pilot study in fiscal 2022 which chemical reagents arewere injected into the ground in an attempt to reduce on-site contamination,contamination. The study will run over a two year period, with a majority of expenses incurred in fiscal 2022. Testing and is currently working with its consultant to design the system.treatment costs of $85 were incurred in fiscal 2023. At this time, the outcome of the pilot study is unknown, but a change in the current remediation strategy, depending on the alternative selected, could result in an increase in future costs and ultimately, an increase in the currently recorded liability, with an offsetting charge to operations in the period recorded. The Company has recorded $300,000$100 as a current liability, and the remaining $616,000$816 is recorded in other non-current liabilities in the consolidated balance sheet.
On March 6, 2020, thesheet as of May 31, 2023.

The Company receivedpreviously disclosed an administrative subpoena fromongoing investigation by the U.S. Treasury Department’s Office of Foreign Assets Control (OFAC) regarding activities or transactions involving parties located in Iran. The Company subsequently conducted an internal investigation under the direction of outside legal counsel and disclosed information concerning certain genomic testing services provided to an unrelated U.S.-based party engaged in veterinary activities involving an Iranian party. The Company continues to cooperate with OFAC’s investigation and is currently examining whether certain of these activities may be eligible for OFAC General Licenses authorizing agricultural and veterinary activities.

F-27

In addition to responding to the administrative subpoena, the Company is implementing additional compliance measures to prevent inadvertent dealings with restricted countries or parties. These measures will further enhance the Company’s international trade compliance program, which is designed to assure that the Company does not conduct business directly or indirectly with any countries or parties subject to U.S. economic sanctions and export control laws. Although it is too early to predict what action, if any, that OFAC will take, the Company does not currently have any reason to believe that OFAC’s pending investigation will have a material impact on its operations, the results of operations for any future period, or its overall financial condition. In fiscal year 2020, the Company tookrecorded a charge to expenseOther (expense) income and recorded a reserve of $600,000$600 to provide for potential fines or penalties on this matter. At this time,On March 28, 2023, the Company believes that itreceived a Cautionary Letter from OFAC concluding its investigation without civil monetary penalty or other enforcement action. As the investigation is adequately reserved for this issue.
effectively resolved, the Company reversed a $600 accrual in the fourth quarter of 2023.

F-30


The Company has agreements with unrelated third parties that provide for the payment of royalties on the sale of certain products. Royalty expense, recorded in sales and marketing, under the terms of these agreements was $2,129,000

$3,392,
$2,524,0001,999, and $2,795,000$2,129 for fiscal years 2021, 20202023, 2022, and 2019,2021, respectively. Some of these agreements provide for guaranteed minimum royalty payments to be paid each fiscal year by the Company for certain technologies. Future minimum royalty payments are as follows: 2022—2024—$115,000, 2023—112, 2025—$110,000, 202
4
109, 2026—$110,000, 202
5
84, 2027—$110,000
84, and
202
6
2028—$85,000
67.

The Company is subject to certain legal and other proceedings in the normal course of business that, in the opinion of management, are not expected to have a material effect on its future results of operations or financial position.

8.
Defined Contribution Benefit Plan

8. Defined Contribution Benefit Plan

The Company maintains a defined contribution 401(k) benefit plan covering substantially all domestic employees. Employees are permitted to defer compensation up to IRS limits, with Neogen matching 100%100% of the first 3% of deferred compensation and 50%50% of the next 2% of deferred compensation.

In the first quarter of fiscal 2021, the Company suspended the 401(k) match, while we assessed the potential financial impact of COVID-19 on the Company. The match was restored in September 2020. 
Neogen’s expense under this plan was $1,204,000, $1,535,000,$2,439, $1,834, and $1,361,000$1,204 in fiscal years 2023, 2022, and 2021, 2020respectively.

9. Fair Value and 2019, respectively.

Derivatives

Fair Value of Financial Instruments

Fair value measurements are determined based upon the exit price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants exclusive of any transaction costs. The Company utilizes a fair value hierarchy based upon the observability of inputs used in valuation techniques as follows:

9.
Segment Information

Level 1:

Observable inputs such as quoted prices in active markets;

Level 2:

Inputs, other than quoted prices in active markets, that are observable either directly or indirectly; and

Level 3:

Unobservable inputs in which there is little or no market data, which require the reporting entity to develop its own assumptions.

The carrying amounts of the Company’s financial instruments other than cash equivalents and marketable securities, which include accounts receivable and accounts payable, approximate fair value based on either their short maturity or current terms for similar instruments.

Items Measured at Fair Value on a Recurring Basis

We forecast our net exposure in various receivables and payables to fluctuations in the value of various currencies, and have entered into a number of foreign currency forward contracts each month to mitigate that exposure. These contracts are recorded net at fair value on our consolidated balance sheets, classified as Level 2 in the fair value hierarchy.

Gains and losses from these foreign currency forward contracts are recognized in other income in our consolidated statements of income (loss). The notional amount of forward contracts in place was $15,500 and $4,424 as of May 31, 2023 and 2022, respectively, and consisted of hedges of transactions up to June 2023.

Fair Value of Derivatives Not Designated as Hedging Instruments

 

Balance Sheet Location

 

May 31, 2023

 

 

May 31, 2022

 

Foreign currency forward contracts, net

 

Other receivable (Other accruals)

 

$

140

 

 

$

(78

)

We record the fair value of our interest rate swaps on a recurring basis using Level 2 observable market inputs for similar assets or liabilities in active markets.

Fair Value of Derivatives Designated as Hedging Instruments

 

Balance Sheet Location

 

May 31, 2023

 

 

May 31, 2022

 

Interest rate swaps – current

 

Other current assets

 

$

2,087

 

 

$

-

 

Interest rate swaps – non-current

 

Other non-current liabilities

 

 

(4,770

)

 

 

-

 

F-31


Items Measured at Fair Value on a Nonrecurring Basis

In addition to items that are measured at fair value on a recurring basis, the Company measures certain assets and liabilities at fair value on a nonrecurring basis, which are not included in the table above. As these nonrecurring fair value measurements are generally determined using unobservable inputs, these fair value measurements are classified within Level 3 of the fair value hierarchy. For further information see Note 2 "Goodwill and Other Intangible Assets" and Note 3 “Business Combinations”.

Items Not Carried at Fair Value

Fair values of the Company’s Term Loan and Senior Notes were as follows:

 

 

May 31, 2023

 

Aggregate fair value

 

$

927,720

 

Aggregate carrying value (1)

 

 

900,000

 

(1) Excludes unamortized debt issuance costs.

Fair values were based on available market information and other observable data and are classified within Level 2 of the fair value hierarchy.

Derivatives

Derivatives Not Designated as Hedging Instruments

The location and amount of gains from derivatives not designated as hedging instruments in our consolidated statements of income (loss) were as follows:

 

Location in statements

 

Year Ended May 31

 

Derivatives Not Designated as Hedging Instruments

 

of (loss) income

 

May 31, 2023

 

 

May 31, 2022

 

 

May 31, 2021

 

Foreign currency forward contracts

 

Other (expense) income

 

$

(10,092

)

 

$

1,218

 

 

$

2,651

 

Derivatives Designated as Hedging Instruments

In November 2022, we entered into a receive-variable, pay-fixed interest rate swap agreement with an initial $250,000 notional value, which is designated as a cash flow hedge. This agreement fixed a portion of the variable interest due on our term loan facility, with an effective date of December 2, 2022 and a maturity date of June 30, 2027. Under the terms of the agreement, we pay a fixed interest rate of 4.215% plus an applicable margin ranging between 150 to 225 basis points and receive a variable rate of interest based on term SOFR from the counterparty, which is reset according to the duration of the SOFR term. The fair value of the interest rate swap as of May 31, 2023 was a net liability of $2,683. The Company expects to reclassify a $2,087 gain of accumulated other comprehensive income into earnings in the next 12 months.

The following table summarizes the other comprehensive income (loss) before reclassifications of derivative gains and losses:

 

 

Other Comprehensive Income (Loss) Before Reclassifications During

 

 

 

Year Ended May 31

 

Derivatives Designated as Hedging Instruments

 

2023

 

 

2022

 

 

2021

 

Interest rate swaps

 

$

(1,599

)

 

$

 

 

$

 

The following table summarizes the reclassification of derivative gains and losses into net income from accumulated other comprehensive income (loss):

F-32


 

 

 

 

Gain (Loss) Reclassified During

 

 

 

Location of Gain (Loss)

 

Year Ended May 31

 

Derivatives Designated as Hedging Instruments

 

Reclassified

 

2023

 

 

2022

 

 

2021

 

Interest rate swaps

 

Interest expense

 

$

440

 

 

$

 

 

$

 

10. Segment Information

The Company has 2two reportable segments: Food Safety and Animal Safety. The Food Safety segment is primarily engaged in the development, production and marketing of diagnostic test kits and related products used by food producers and processors to detect harmful natural toxins, foodborne bacteria, allergens and levels of general sanitation. The Animal Safety segment is primarily engaged in the development, production and marketing of products dedicated to animal safety, including a complete line of consumable products marketed to veterinarians and animal health product distributors; thisdistributors. This segment also provides genomic identification and related interpretive bioinformatic services. Additionally, the Animal Safety segment produces and markets rodenticides,rodent control products, disinfectants and insecticidesinsect control products to assist in the control of rodents, insects and disease in and around agricultural, food production and other facilities.

Neogen’s international operations in the United Kingdom, Mexico, Guatemala, Brazil, Argentina, Uruguay, Chile, China and India originally focused on the sales and marketing of our food safety products, and each of these units reports through the Food Safety segment. In recent years, these operations have expanded to offer the Company’s complete line of products and services, including those usually associated with the Animal Safety segment such as cleaners, disinfectants, rodenticides, insecticides,rodent control products, insect control products, veterinary instruments and genomics services. These additional products and services are managed and directed by existing management and are reported through the Food Safety segment.

Neogen’s operation in Australia originally focused on providing genomics services and sales of animal safety products and reports through the Animal Safety segment. With the acquisition of Cell BioSciences in February 2020, thisThis operation has expanded to offer our complete line of products and services, including those usually associated with the Food Safety segment. These additional products are managed and directed by existing management at Neogen Australasia and report through the Animal Safety segment.

The accounting policies of each of the segments are the same as those described in Note 1.

F-28

Significant Accounting Policies".

F-33


Segment information is as follows:

 

 

Food Safety

 

 

Animal Safety

 

 

Corporate and
Eliminations
(1)

 

 

Total

 

Fiscal 2023

 

 

 

 

 

 

 

 

 

 

 

 

Product revenues, net to external customers

 

$

518,488

 

 

$

196,588

 

 

$

 

 

$

715,076

 

Service revenues, net to external customers

 

 

28,309

 

 

 

79,062

 

 

 

 

 

 

107,371

 

Total revenues to external customers

 

 

546,797

 

 

 

275,650

 

 

 

 

 

 

822,447

 

Operating income (loss)

 

 

60,414

 

 

 

43,332

 

 

 

(66,231

)

 

 

37,515

 

Depreciation and amortization

 

 

76,841

 

 

 

11,536

 

 

 

 

 

 

88,377

 

Interest expense

 

 

 

 

 

 

 

 

55,961

 

 

 

55,961

 

Total assets

 

 

3,970,356

 

 

 

338,507

 

 

 

245,569

 

 

 

4,554,432

 

Expenditures for long-lived assets

 

 

52,169

 

 

 

13,588

 

 

 

 

 

 

65,757

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Fiscal 2022

 

 

 

 

 

 

 

 

 

 

 

 

Product revenues, net to external customers

 

$

231,626

 

 

$

193,038

 

 

$

 

 

$

424,664

 

Service revenues, net to external customers

 

 

28,353

 

 

 

74,142

 

 

 

 

 

 

102,495

 

Total revenues to external customers

 

 

259,979

 

 

 

267,180

 

 

 

 

 

 

527,159

 

Operating income (loss)

 

 

38,581

 

 

 

52,546

 

 

 

(32,509

)

 

 

58,618

 

Depreciation and amortization

 

 

13,386

 

 

 

10,308

 

 

 

 

 

 

23,694

 

Interest expense

 

 

 

 

 

 

 

 

72

 

 

 

72

 

Total assets

 

 

304,461

 

 

 

307,417

 

 

 

381,051

 

 

 

992,929

 

Expenditures for long-lived assets

 

 

7,842

 

 

 

16,939

 

 

 

 

 

 

24,781

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Fiscal 2021

 

 

 

 

 

 

 

 

 

 

 

 

Product revenues, net to external customers

 

$

209,104

 

 

$

167,198

 

 

$

 

 

$

376,302

 

Service revenues, net to external customers

 

 

25,140

 

 

 

67,017

 

 

 

 

 

 

92,157

 

Total revenues to external customers

 

 

234,244

 

 

 

234,215

 

 

 

 

 

 

468,459

 

Operating income (loss)

 

 

33,725

 

 

 

48,685

 

 

 

(8,241

)

 

 

74,169

 

Depreciation and amortization

 

 

11,575

 

 

 

9,466

 

 

 

 

 

 

21,041

 

Interest expense

 

 

 

 

 

 

 

 

78

 

 

 

78

 

Total assets

 

 

295,065

 

 

 

244,039

 

 

 

381,088

 

 

 

920,192

 

Expenditures for long-lived assets

 

 

13,730

 

 

 

12,982

 

 

 

 

 

 

26,712

 

(1)
(in thousands)
  
Food Safety
   
Animal Safety
   
Corporate and
Eliminations (1)
  
Total
 
Fiscal 2021
                   
Product revenues to external customers
  $209,104   $167,198   $  $376,302 
Service revenues to external customers
   25,140    67,017       92,157 
                    
Total revenues to external customers
   234,244    234,215       468,459 
Operating income (loss)
   33,725    48,685    (8,241)    74,169 
Depreciation and amortization
   11,575    9,466       21,041 
Total Assets
   295,065    244,039    381,088   920,192 
Expenditures for long-lived assets
   13,730    12,982       26,712 
     
Fiscal 2020
                   
Product revenues to external customers
  $189,893   $145,646   $—    $335,539 
Service revenues to external customers
   22,798    59,833    —     82,631 
                    
Total revenues to external customers
   212,691    205,479    —     418,170 
Operating income (loss)
   33,526    39,051    (5,054  67,523 
Depreciation and amortization
   10,173    8,223    —     18,396 
Total Assets
   222,331    231,178    343,673   797,182 
Expenditures for long-lived assets
   15,867    8,185    —     24,052 
     
Fiscal 2019
                   
Product revenues to external customers
  $190,675   $148,764   $—    $339,439 
Service revenues to external customers
   22,799    51,948    —     74,747 
                    
Total revenues to external customers
   213,474    200,712    —     414,186 
Operating income (loss)
   39,020    33,875    (4,801  68,094 
Depreciation and amortization
   9,525    8,099    —     17,624 
Total Assets
   206,267    221,950    267,523   695,740 
Expenditures for long-lived assets
   8,916    5,745    —     14,661 
(1)
Includes corporate assets, including cash and cash equivalents, marketable securities, current and deferred tax accounts, and overhead expenses not allocated to specific business segments. Also includes the elimination of intersegment transactions and
non-controlling
interests.
Includes corporate assets, including cash and cash equivalents, marketable securities, current and deferred tax accounts, and overhead expenses not allocated to specific business segments. Also includes the elimination of intersegment transactions.

Revenue is determined by location of the end customer. The following table presents the Company’s revenue disaggregated by geographical location:location.

 

Year ended May 31

 

 

 

2023

 

 

2022

 

 

2021

 

Domestic

 

$

424,005

 

 

$

317,820

 

 

$

285,262

 

International

 

 

398,442

 

 

 

209,339

 

 

 

183,197

 

Total revenue

 

$

822,447

 

 

$

527,159

 

 

$

468,459

 

The following table presents the Company's net property and equipment amounts disaggregated by country.

 

Year ended May 31

 

 

 

2023

 

 

2022

 

United States

 

$

130,967

 

 

$

63,313

 

United Kingdom

 

 

20,123

 

 

 

14,204

 

Other

 

 

47,659

 

 

 

33,067

 

Total PPE

 

$

198,749

 

 

$

110,584

 

   
Year ended May 31
 
(in thousands)
  
2021
   
2020
 
Domestic
  $285,262   $253,458 
International
   183,197    164,712 
           
Total revenue
  $468,459   $418,170 
           
10.
Stock Repurchases
In October 2018, the Company’s Board of Directors passed a resolution terminating the Company’s prior stock buyback program, which had been approved in December 2008, and authorized a new program to purchase, subject to market conditions, up to 6,000,000 shares of the Company’s common stock. In December 2018, the Company purchased 100,000 shares under the new program in open market transactions for a total price, including commissions, of $3,134,727. Shares acquired under the program were retired. A total of 5,900,000 shares of common stock remained available for repurchase under this program as of May 31, 2021.
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11.
Summary of Quarterly Data (Unaudited)
   
Quarter Ended
 
(in thousands, except per share)
  
August
2020
   
November
2020
   
February
2021
   
May
2021
 
Total Revenue
  $109,325   $115,000   $116,709   $127,425 
Gross Margin
   50,302    53,214    53,849    57,691 
Net income
   15,860    15,885    13,377    15,760 
Basic net income per share
  $0.15   $0.15   $0.13   $0.15 
Diluted net income per share
  $0.15   $0.15   $0.12   $0.15 
  
   
Quarter Ended
 
(in thousands, except per share)
  
August
2019
   
November
2019
   
February
2020
   
May
2020
 
Total Revenue
  $101,424   $107,803   $99,869   $109,074 
Gross Margin
   48,194    51,026    45,330    51,729 
Net income
   14,652    16,276    12,200    16,347 
Basic net income per share
  $0.14   $0.15   $0.12   $0.15 
Diluted net income per share
  $0.14   $0.15   $0.11   $0.15 
Quarterly net income per share is based on weighted-average shares outstanding and potentially dilutive stock options for the specific period and as a result, will not necessarily aggregate to total net income per share as computed for the year as disclosed in the consolidated statements of income.
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