FDA inspection
Teva Pharmaceuticals USA Inc: FDA inspection ending Dec 18, 2001
FDA inspection 243185 · No Action Indicated (NAI) · Mexico, MO
Key facts
| Inspection ID | 243185 |
|---|---|
| Firm | Teva Pharmaceuticals USA Inc |
| FEI number | 1938125 |
| Address | 5000 Snyder Dr |
| City | Mexico |
| State | MO |
| ZIP | 65265-8917 |
| Fiscal year | 2002 |
| Inspection end date | Dec 18, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| 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
- 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