FDA Inspection 1115202 — FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office

FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office — FEI 3010516924

The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office on Sep 12, 2019 in Hitachiomiya. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Sep 12, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Hitachiomiya (Japan)

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