FDA inspection
Huvepharma Inc.: FDA inspection ending Sep 1, 2015
FDA inspection 950798 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 950798 |
|---|---|
| Firm | Huvepharma Inc. |
| FEI number | 1940172 |
| Address | 3360 Maury Ave |
| City | Saint Louis |
| State | MO |
| ZIP | 63116 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Sep 1, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data