FDA Inspection 918251 — Circassia AB

Circassia AB — FEI 3008662397

The FDA completed an inspection of Circassia AB on Feb 18, 2015 in Uppsala. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 18, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Uppsala (Sweden)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.