FDA inspection
GMP Laboratories of America Inc: FDA inspection ending Jan 14, 2020
FDA inspection 1115118 · Voluntary Action Indicated (VAI) · Anaheim, CA
Key facts
| Inspection ID | 1115118 |
|---|---|
| Firm | GMP Laboratories of America Inc |
| FEI number | 3002710875 |
| Address | 2931 E La Jolla St |
| City | Anaheim |
| State | CA |
| ZIP | 92806 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Jan 14, 2020 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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