FDA Inspection 837192 — Fujifilm Corporation

Fujifilm Corporation — FEI 3001722928

The FDA completed an inspection of Fujifilm Corporation on Apr 25, 2013 in Ashigarakami-Gun. 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
Apr 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Ashigarakami-Gun (Japan)

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