FDA Inspection 797599 — Circassia AB

Circassia AB — FEI 3008662397

The FDA completed an inspection of Circassia AB on September 6, 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
September 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Uppsala (Sweden)