FDA Inspection 998293 — Oculus Optikgeraete GMBH
The FDA completed an inspection of Oculus Optikgeraete GMBH on Nov 10, 2016 in Wetzlar. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 10, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wetzlar (Germany)