FDA inspection
Actavis Laboratories UT, Inc.: FDA inspection ending Jun 8, 2012
FDA inspection 787151 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 787151 |
|---|---|
| Firm | Actavis Laboratories UT, Inc. |
| FEI number | 1000117147 |
| Address | 577 S Chipeta Way |
| City | Salt Lake City |
| State | UT |
| ZIP | 84108 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Jun 8, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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
- 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