FDA Warning Letter — Terumo Medical Corporation

Case 483231 — FEI 1118880

The FDA took a Warning Letter action against Terumo Medical Corporation on March 17, 2016 (Elkton, MD). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Terumo Medical Corporation
Date
March 17, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Elkton, MD (United States)