FDA Warning Letter — Unisis Corp.

Case 327798 — FEI 3003803331

The FDA took a Warning Letter action against Unisis Corp. on September 7, 2012 (Koshigaya, Japan). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Unisis Corp.
Date
September 7, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Koshigaya (Japan)