FDA inspection
GCP Laboratories: FDA inspection ending Mar 13, 2002
FDA inspection 208199 · No Action Indicated (NAI) · Gulfport, MS
Key facts
| Inspection ID | 208199 |
|---|---|
| Firm | GCP Laboratories |
| FEI number | 1019058 |
| Address | 3600 25th Ave |
| City | Gulfport |
| State | MS |
| ZIP | 39501-6922 |
| Fiscal year | 2002 |
| Inspection end date | Mar 13, 2002 |
| 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
- 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