Warning letter
Virbac Inc.: warning letter of Dec 10, 2008
FDA warning letter 38578 · Kansas City District Office
Key facts
| Reference number | 38578 |
|---|---|
| Company | Virbac Inc. |
| Subject | CGMP For Manufacturing, Packing, Storage or Installation/Adulterated/Misbranded |
| Issue date | Dec 10, 2008 |
| Posted date | Dec 10, 2008 |
| Issuing office | Kansas City District Office |
| Product type | Veterinary |
| CFR sections cited | 211.192, 202.1, 211.22(a), 211.100(b), 211.160(b), 211.160(b)(4) |
| Inspection city | Bridgeton |
| Inspection ZIP | 63044-2421 |
| Inspection start date | Jul 21, 2008 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: