FDA inspection
Gelita USA, Inc.: FDA inspection ending Aug 28, 2014
FDA inspection 897258 · Voluntary Action Indicated (VAI) · Sergeant Bluff, IA
Key facts
| Inspection ID | 897258 |
|---|---|
| Firm | Gelita USA, Inc. |
| FEI number | 1920862 |
| Address | 2445 Port Neal Industrial Rd |
| City | Sergeant Bluff |
| State | IA |
| ZIP | 51054 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Aug 28, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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