FDA inspection
Actavis South Atlantic LLC: FDA inspection ending Apr 19, 2012
FDA inspection 783901 · No Action Indicated (NAI) · Sunrise, FL
Key facts
| Inspection ID | 783901 |
|---|---|
| Firm | Actavis South Atlantic LLC |
| FEI number | 3004090892 |
| Address | 13800 NW 2nd St Ste 190 |
| City | Sunrise |
| State | FL |
| ZIP | 33325 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Apr 19, 2012 |
| 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
- No 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