FDA inspection
Actavis Elizabeth LLC, A Company of Teva: FDA inspection ending May 12, 2005
FDA inspection 379362 · Voluntary Action Indicated (VAI) · Elizabeth, NJ
Key facts
| Inspection ID | 379362 |
|---|---|
| Firm | Actavis Elizabeth LLC, A Company of Teva |
| FEI number | 2211563 |
| Address | 200 Elmora Ave |
| City | Elizabeth |
| State | NJ |
| ZIP | 07202-1106 |
| Fiscal year | 2005 |
| Inspection end date | May 12, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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
- 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