FDA Inspection 885791 — Huvepharma Inc.
The FDA completed an inspection of Huvepharma Inc. on July 2, 2014 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 2, 2014
- Fiscal Year
- 2014
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Saint Louis, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1227 | 21 CFR 211.67(c) | Cleaning/maintenance records not kept |
| 2379 | 21 CFR 226.40(e) | Cleaning to prevent contamination of Type A articles |
| 2416 | 21 CFR 226.80(b)(2) | Label examination |
| 2421 | 21 CFR 226.110 | Records maintenance |
| 4155 | 21 CFR 226.115 | Appropriate action not taken |