FDA inspection
Unifi: FDA inspection ending Jun 16, 2010
FDA inspection 668737 · No Action Indicated (NAI) · Des Moines, IA
Key facts
| Inspection ID | 668737 |
|---|---|
| Firm | Unifi |
| FEI number | 3002964664 |
| Address | 5800 Fleur Dr <DSM>, Suite 208 |
| City | Des Moines |
| State | IA |
| ZIP | 50321 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jun 16, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Technical Assistance: Food and Cosmetics |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No 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