FDA Inspection 853199 — Oculus Optikgeraete GMBH
The FDA completed an inspection of Oculus Optikgeraete GMBH on Sep 19, 2013 in Wetzlar. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 19, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wetzlar (Germany)