FDA inspection
Gelita USA Inc.-Chicago: FDA inspection ending Jul 11, 2003
FDA inspection 281502 · No Action Indicated (NAI) · Calumet City, IL
Key facts
| Inspection ID | 281502 |
|---|---|
| Firm | Gelita USA Inc.-Chicago |
| FEI number | 1419670 |
| Address | 10 Wentworth Ave |
| City | Calumet City |
| State | IL |
| ZIP | 60409-2744 |
| Fiscal year | 2003 |
| Inspection end date | Jul 11, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazard |
| 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