FDA Inspection 839344 — R82 A/S
The FDA completed an inspection of R82 A/S on Jun 7, 2013 in Gedved. 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
- Jun 7, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gedved (Denmark)