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483
•Virbac Corporation•November 25, 2019

Virbac Corporation – FDA 483, Nov 25, 2019

Record Details

An FDA inspection of Virbac Corporation, an animal drug manufacturer in Bridgeton, MO, revealed significant deficiencies in laboratory controls and investigation procedures. The firm lacked scientifically sound test methods for product impurities, failed to properly investigate out-of-specification results and product contamination, and exhibited poor data integrity practices. These issues indicate a systemic breakdown in quality control for their animal drug products.

Company
Virbac Corporation
Inspection date
November 25, 2019
Product type
veterinary
Office
Division of Human and Animal Food Operations - West II
People
  • Lisa L. Flores (Consumer Safety Officer/ Federal Investigator)
  • Robert J. Ham (Investigator?)
View Company Profile

ID · 7dbe3135-33c0-44cb-851d-8dc8079a2b05

Other documents for Virbac Corporation
  • 483 - 2026-01-22January 22, 2026
  • 483 - 2023-07-28July 28, 2023

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