FDA Inspection
Neogen CorporationNeogen Corporation – FDA Inspection, Jan 11, 2018
Record Details
This FDA Inspection record concerns Neogen Corporation, with an inspection on January 11, 2018, issued by the Center for Veterinary Medicine, covering veterinary.
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ID · 5445d156-7fd0-474b-a9e5-71bcdfb4c638
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1037465
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 211.194(a)(4)Complete Test Data
- 21 CFR 211.113(a)Procedures for non-sterile drug products
- 21 CFR 211.160(a)Lab controls established, including changes
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of Neogen Corporation
11| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2026 | Not classified | Cincinnati District Office | Drug Quality Assurance |
| December 21, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 27, 2022 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| March 16, 2021 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| April 28, 2016 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Neogen Corporation
- FDA Inspection 1306238 - 2026-03-06
- FDA Inspection 1225713 - 2023-12-21
- FDA Inspection 1190704 - 2022-10-27
- FDA Inspection 1136685 - 2021-03-16
- FDA Inspection 969530 - 2016-04-28
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