FDA Inspection 1008948 — Ophtec BV
The FDA completed an inspection of Ophtec BV on Mar 23, 2017 in Groningen. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Mar 23, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Groningen (Netherlands)