FDA Inspection 1115949 — Fujifilm Corporation

Fujifilm Corporation — FEI 3001722928

The FDA completed an inspection of Fujifilm Corporation on September 30, 2019 in Ashigarakami-Gun. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 30, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Ashigarakami-Gun (Japan)