FDA Inspection 918251 — Circassia AB

Circassia AB — FEI 3008662397

The FDA completed an inspection of Circassia AB on February 18, 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 18, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Uppsala (Sweden)