FDA inspection
Oculus Optikgeraete GMBH: FDA inspection ending Sep 19, 2013
FDA inspection 853199 · Voluntary Action Indicated (VAI) · Wetzlar
Key facts
| Inspection ID | 853199 |
|---|---|
| Firm | Oculus Optikgeraete GMBH |
| FEI number | 3002807782 |
| Address | Munchholzhauser Str. 29 |
| City | Wetzlar |
| Country | Germany |
| Fiscal year | 2013 |
| Inspection end date | Sep 19, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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