FDA inspection
Dornier Medtech GmbH: FDA inspection ending Dec 14, 2022
FDA inspection 1194137 · No Action Indicated (NAI) · Wessling
Key facts
| Inspection ID | 1194137 |
|---|---|
| Firm | Dornier Medtech GmbH |
| FEI number | 3002806833 |
| Address | Argelsrieder Feld 7 |
| City | Wessling |
| Country | Germany |
| Fiscal year | 2023 |
| Inspection end date | Dec 14, 2022 |
| 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