FDA Warning Letter — FUJIFILM Healthcare Americas Corporation

Case 470470 — FEI 2431293

The FDA took a Warning Letter action against FUJIFILM Healthcare Americas Corporation on August 12, 2015 (Wayne, NJ). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
FUJIFILM Healthcare Americas Corporation
Date
August 12, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Wayne, NJ (United States)