Warning letter
Performance Products Inc: warning letter of Nov 20, 2012
FDA warning letter 348807 · Kansas City District Office
Key facts
| Reference number | 348807 |
|---|---|
| Company | Performance Products Inc |
| Subject | CGMP/Finished Pharmaceuticals/Animal Drugs/Misbranded |
| Issue date | Nov 20, 2012 |
| Posted date | Nov 20, 2012 |
| Issuing office | Kansas City District Office |
| Product type | Veterinary |
| CFR sections cited | 211.67(b), 211.68(a), 211.84(d)(1), 211.100(a), 211.166(a), 211.180(c) |
| Inspection city | Saint Louis |
| Inspection ZIP | 63110 |
| Inspection start date | Jul 16, 2012 |
| 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: