FDA inspection
Provimi North America, Inc.: FDA inspection ending Mar 25, 2008
FDA inspection 511728 · No Action Indicated (NAI) · Weatherford, TX
Key facts
| Inspection ID | 511728 |
|---|---|
| Firm | Provimi North America, Inc. |
| FEI number | 1000516203 |
| Address | 1050 Vigortone Blvd |
| City | Weatherford |
| State | TX |
| ZIP | 76086-1554 |
| Fiscal year | 2008 |
| Inspection end date | Mar 25, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Monit of Marketed Animal Drug,Feed &Dev |
| Product type | Drugs |
At a glance
- None Citations
- None 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