FDA inspection
Dornier Medtech GmbH: FDA inspection ending Apr 29, 2011
FDA inspection 726892 · Official Action Indicated (OAI) · Wessling
Key facts
| Inspection ID | 726892 |
|---|---|
| Firm | Dornier Medtech GmbH |
| FEI number | 3002806833 |
| Address | Argelsrieder Feld 7 |
| City | Wessling |
| Country | Germany |
| Fiscal year | 2011 |
| Inspection end date | Apr 29, 2011 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 203432 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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