Virbac Corporation
FDA inspection history across 2 sites, 2008 to 2023
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2008: one warning letter; 2019: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2008One warning letter, at Fort Worth, Texas.
- 2019One Form 483, at Bridgeton, Missouri.
- 2019The longest 483 on file: 2 observations over 4 pages at Bridgeton, Missouri.
- 2023One Form 483, at Bridgeton, Missouri.
Cited most
Across all Virbac observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete Virbac file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Bridgeton, Missouri
Two Form 483s · 2019 to 2023 · 3 observations
Latest: Form 483, Jul 28, 2023 →Fort Worth, Texas
One warning letter · 2008
Latest: Warning letter, Dec 10, 2008 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-07-28 | 483 Form 483 | Bridgeton, Missouri | 1 | $99 |
| 2019-11-25 | 483 Form 483 | Bridgeton, Missouri | 2 | $99 |
| 2008-12-10 | Warning letter Warning letter | Fort Worth, Texas | — | $99 |
Investigators on these documents
FEI number 1944921 · most recent document Jul 28, 2023
About Virbac Corporation
How many FDA Form 483s has Virbac Corporation received?
FDA Intel has 2 Form 483s on file for Virbac Corporation; the most recent is dated Jul 28, 2023.
When was Virbac Corporation last inspected by FDA?
The most recent FDA inspection document on file for Virbac Corporation is a Form 483 dated Jul 28, 2023, for the site in Bridgeton, Missouri.
What did FDA cite at Virbac Corporation?
The regulations cited most in the observations on file for Virbac Corporation are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.
Has Virbac Corporation received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Virbac Corporation; the most recent is dated Dec 10, 2008.