# Neogen Corporation - Inspection Records

Source: https://www.keypedia.com/companies/neogen-corporation/16592aaf-11fc-4c34-b764-6b8fb555268e

> Inspection records and compliance data for Neogen Corporation in Lexington, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Neogen Corporation
- FEI Number: 3009631819
- City: Lexington
- State: Kentucky
- Country Name: United States
- Address Line 1: 1847 Mercer Rd Ste A
- Zip Code: 40511

## Related Documents

- [FDA Inspection 1306238 - Neogen Corporation - 2026-03-06](https://www.keypedia.com/records/fda_inspections/neogen-corporation/3fb0a22b-d494-4fff-a5ed-8370f8744617) — source: FDA, date: March 6, 2026
- [FDA Inspection 1306238 - Neogen Corporation - 2026-03-06](https://www.keypedia.com/records/fda_inspections/neogen-corporation/8e8601fa-6479-4129-be2c-1dd584b36cc6) — source: FDA, date: March 6, 2026
- [FDA Inspection 1306238 - Neogen Corporation - 2026-03-06](https://www.keypedia.com/records/fda_inspections/neogen-corporation/ac9c1fa8-991a-4371-a46b-d733f8d9428d) — source: FDA, date: March 6, 2026
- [483 - Neogen Corporation - 2023-12-21](https://www.keypedia.com/records/483/neogen-corporation/7516b342-364e-4d46-8daa-26a7a0eaa5cd) — source: FDA, date: December 21, 2023
- [FDA Inspection 1225713 - Neogen Corporation - 2023-12-21](https://www.keypedia.com/records/fda_inspections/neogen-corporation/31ccc7c2-f51a-4ab9-aa7e-25042bf988de) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2023
- [FDA Inspection 1225713 - Neogen Corporation - 2023-12-21](https://www.keypedia.com/records/fda_inspections/neogen-corporation/0f7217af-829f-4dc8-ba41-cc7f90f696db) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2023
- [FDA Inspection 1190704 - Neogen Corporation - 2022-10-27](https://www.keypedia.com/records/fda_inspections/neogen-corporation/6a9732e3-7172-40c1-b907-4606806aa875) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2022
- [483 - Neogen Corporation - 2021-03-16](https://www.keypedia.com/records/483/neogen-corporation/29796c36-3e69-4d39-87b0-293fe9baa378) — source: FDA, date: March 16, 2021
- [FDA Inspection 1136685 - Neogen Corporation - 2021-03-16](https://www.keypedia.com/records/fda_inspections/neogen-corporation/6d06cb01-4114-4439-b029-22c112453a73) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 16, 2021
- [FDA Inspection 1037465 - Neogen Corporation - 2018-01-11](https://www.keypedia.com/records/fda_inspections/neogen-corporation/5445d156-7fd0-474b-a9e5-71bcdfb4c638) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 11, 2018
- [FDA Inspection 969530 - Neogen Corporation - 2016-04-28](https://www.keypedia.com/records/fda_inspections/neogen-corporation/a4bca5f7-8b0a-4f4e-9d5d-5911ebc497cd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2016
- [FDA Inspection 903658 - Neogen Corporation - 2014-11-17](https://www.keypedia.com/records/fda_inspections/neogen-corporation/8bf5df25-c019-4f20-9d96-2e9e339590b7) — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2014

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