FDA inspection
Degudent GmbH: FDA inspection ending Jul 23, 2009
FDA inspection 601611 · Voluntary Action Indicated (VAI) · Hanau
Key facts
| Inspection ID | 601611 |
|---|---|
| Firm | Degudent GmbH |
| FEI number | 3003999430 |
| Address | Rodenbacher Chaussee 4 |
| City | Hanau |
| Country | Germany |
| Fiscal year | 2009 |
| Inspection end date | Jul 23, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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