FDA inspection
Teva Pharmaceuticals USA Inc: FDA inspection ending Feb 9, 2012
FDA inspection 768901 · Voluntary Action Indicated (VAI) · Mexico, MO
Key facts
| Inspection ID | 768901 |
|---|---|
| Firm | Teva Pharmaceuticals USA Inc |
| FEI number | 1938125 |
| Address | 5000 Snyder Dr |
| City | Mexico |
| State | MO |
| ZIP | 65265 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Feb 9, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 1–9 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