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FDA Inspection
•Neogen Corporation•May 23, 2013

Neogen Corporation – FDA Inspection, May 23, 2013

Record Details

This FDA Inspection record concerns Neogen Corporation, with an inspection on May 23, 2013, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Neogen Corporation
Inspection Date
May 23, 2013
Product Type
Veterinary
Office
Center for Veterinary Medicine
View Company Profile

ID · 7a2d03a7-3c14-4bcd-a66c-04cd0e573440

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
836498
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

FDA Citations

4
  1. 21 CFR 211.166(b)Adequate number of batches on stability
  2. 21 CFR 211.192Investigations of discrepancies, failures
  3. 21 CFR 211.180(e)(1)Review of representative number of batches
  4. 21 CFR 211.80(a)Written Procedures Not Followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Neogen Corporation

11
DateClassificationOfficeProject area
March 6, 2026Not classifiedCincinnati District OfficeDrug Quality Assurance
December 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 27, 2022NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 16, 2021VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 11, 2018VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 11 other inspections on the company page
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 1037465 - 2018-01-11

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