FDA inspection
Provimi North America, Inc.: FDA inspection ending Feb 3, 2016
FDA inspection 956591 · No Action Indicated (NAI) · Weatherford, TX
Key facts
| Inspection ID | 956591 |
|---|---|
| Firm | Provimi North America, Inc. |
| FEI number | 1000516203 |
| Address | 1050 Vigortone Blvd |
| City | Weatherford |
| State | TX |
| ZIP | 76086-1554 |
| Fiscal year | 2016 |
| Inspection end date | Feb 3, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feeds, and Devices |
| 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