FDA inspection
Acura Pharmaceuticals, Inc.: FDA inspection ending May 20, 2009
FDA inspection 583323 · No Action Indicated (NAI) · Culver, IN
Key facts
| Inspection ID | 583323 |
|---|---|
| Firm | Acura Pharmaceuticals, Inc. |
| FEI number | 1824681 |
| Address | 16235 State Road 17 |
| City | Culver |
| State | IN |
| ZIP | 46511 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | May 20, 2009 |
| 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