FDA inspection
Oculus Optikgeraete GMBH: FDA inspection ending Jun 24, 2010
FDA inspection 675579 · Voluntary Action Indicated (VAI) · Wetzlar
Key facts
| Inspection ID | 675579 |
|---|---|
| Firm | Oculus Optikgeraete GMBH |
| FEI number | 3002807782 |
| Address | Munchholzhauser Str. 29 |
| City | Wetzlar |
| Country | Germany |
| Fiscal year | 2010 |
| Inspection end date | Jun 24, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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