FDA inspection
DMB Apparatebau GmbH: FDA inspection ending Apr 29, 2026
FDA inspection 1317534 · No Action Indicated (NAI) · Worrstadt
Key facts
| Inspection ID | 1317534 |
|---|---|
| Firm | DMB Apparatebau GmbH |
| FEI number | 3005465238 |
| Address | Spiesheimer Weg 25a |
| City | Worrstadt |
| Country | Germany |
| Fiscal year | 2026 |
| Inspection end date | Apr 29, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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