FDA inspection
Gemini PharmChem Mannheim GmbH: FDA inspection ending Feb 19, 2026
FDA inspection 1329494 · Voluntary Action Indicated (VAI) · Mannheim
Key facts
| Inspection ID | 1329494 |
|---|---|
| Firm | Gemini PharmChem Mannheim GmbH |
| FEI number | 3014000756 |
| City | Mannheim |
| Country | Germany |
| Fiscal year | 2026 |
| Inspection end date | Feb 19, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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