FDA inspection
FUJIFILM MEDWORK GMBH: FDA inspection ending Mar 26, 2025
FDA inspection 1264887 · Voluntary Action Indicated (VAI) · Hochstadt A.D.Aisch
Key facts
| Inspection ID | 1264887 |
|---|---|
| Firm | FUJIFILM MEDWORK GMBH |
| FEI number | 3020707080 |
| Address | Medwork Ring 1 |
| City | Hochstadt A.D.Aisch |
| Country | Germany |
| Fiscal year | 2025 |
| Inspection end date | Mar 26, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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