FDA Inspection 933680 — Orkla Care AB

Orkla Care AB — FEI 3000182940

The FDA completed an inspection of Orkla Care AB on June 11, 2015 in Solna. 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 11, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Solna (Sweden)