FDA inspection
Gelita USA Inc.: FDA inspection ending Oct 22, 2018
FDA inspection 1070182 · Sergeant Bluff, IA
Key facts
| Inspection ID | 1070182 |
|---|---|
| Firm | Gelita USA Inc. |
| FEI number | 1920862 |
| Address | 2445 Port Neal Rd |
| City | Sergeant Bluff |
| State | IA |
| ZIP | 51054 |
| Fiscal year | 2019 |
| Inspection end date | Oct 22, 2018 |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None 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