FDA Inspection 573253 — AMO Uppsala AB
The FDA completed an inspection of AMO Uppsala AB on March 19, 2009 in Uppsala. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 19, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Uppsala (Sweden)
Additional Details
Postmarket Audit Inspections