FDA Inspection 1011328 — AMO Uppsala AB
The FDA completed an inspection of AMO Uppsala AB on Apr 5, 2017 in Uppsala. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 5, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Uppsala (Sweden)