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FDA Inspection 1111976 — Virbac Corporation

Virbac Corporation — FEI 1944921

The FDA completed an inspection of Virbac Corporation on November 25, 2019 in Bridgeton, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 25, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bridgeton, MO (United States)

Facility

Other inspections at this facility

  • 1324954 (NAI Wed Jun 03 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1211094 (VAI Fri Jul 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1058067 (NAI Thu Mar 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988049 (VAI Wed Sep 07 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 908575 (OAI Tue Dec 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources