FDA Inspection 567005 — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA completed an inspection of Q-Med AB on January 29, 2009 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
January 29, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Uppsala (Sweden)