FDA inspection
Teva Biopharmaceuticals USA: FDA inspection ending Apr 17, 2013
FDA inspection 829556 · Voluntary Action Indicated (VAI) · Rockville, MD
Key facts
| Inspection ID | 829556 |
|---|---|
| Firm | Teva Biopharmaceuticals USA |
| FEI number | 3007059649 |
| Address | 9410 Key West Ave |
| City | Rockville |
| State | MD |
| ZIP | 20850-3345 |
| Fiscal year | 2013 |
| Inspection end date | Apr 17, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- 1–9 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