FDA Inspection 789285 — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA completed an inspection of Q-Med AB on June 21, 2012 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
June 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Uppsala (Sweden)

Additional Details

Postmarket Audit Inspections