FDA inspection
Tutogen Medical GmbH: FDA inspection ending Jun 25, 2026
FDA inspection 1325500 · No Action Indicated (NAI) · Neunkirchen A. Brand
Key facts
| Inspection ID | 1325500 |
|---|---|
| Firm | Tutogen Medical GmbH |
| FEI number | 3002924436 |
| City | Neunkirchen A. Brand |
| Country | Germany |
| Fiscal year | 2026 |
| Inspection end date | Jun 25, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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