Warning letter
Huvepharma Inc: warning letter of Jun 13, 2013
FDA warning letter 394340 · Kansas City District Office
Key facts
| Reference number | 394340 |
|---|---|
| Company | Huvepharma Inc |
| Subject | Medicated Feed/Adulterated |
| Issue date | Jun 13, 2013 |
| Posted date | Jun 13, 2013 |
| Issuing office | Kansas City District Office |
| Product type | Veterinary |
| CFR sections cited | 226.58(a), 226, 226.20(b), 226.40(b) |
| Inspection city | Saint Louis |
| Inspection ZIP | 63116 |
| Inspection start date | Feb 14, 2013 |
| 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: