FDA Inspection 1048550 — Q-Med AB
The FDA completed an inspection of Q-Med AB on March 29, 2018 in Uppsala. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- March 29, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Uppsala (Sweden)
Additional Details
Postmarket Audit Inspections