FDA Inspection 1005167 — Oculo Plastik, Inc.
The FDA completed an inspection of Oculo Plastik, Inc. on December 7, 2016 in Montreal. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 7, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Montreal (Canada)