FDA Inspection 830218 — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA completed an inspection of Q-Med AB on April 25, 2013 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
April 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Uppsala (Sweden)

Additional Details

Postmarket Audit Inspections