FDA inspection
Teva Branded Pharmaceutical Products R&D, Inc.: FDA inspection ending May 15, 2017
FDA inspection 1017798 · Voluntary Action Indicated (VAI) · West Chester, PA
Key facts
| Inspection ID | 1017798 |
|---|---|
| Firm | Teva Branded Pharmaceutical Products R&D, Inc. |
| FEI number | 3005144136 |
| Address | 145 Brandywine Pkwy |
| City | West Chester |
| State | PA |
| ZIP | 19380-4245 |
| Fiscal year | 2017 |
| Inspection end date | May 15, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 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