FDA Inspection 678939 — Q-Med AB
The FDA completed an inspection of Q-Med AB on Jul 9, 2010 in Uppsala. 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
- Jul 9, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Uppsala (Sweden)