FDA Inspection 921654 — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA completed an inspection of Q-Med AB on February 13, 2015 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
February 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Uppsala (Sweden)