FDA Warning Letter — ITG-Medev, Inc.

Case 562975 — FEI 1000307251

The FDA took a Warning Letter action against ITG-Medev, Inc. on September 7, 2018 (San Francisco, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
ITG-Medev, Inc.
Date
September 7, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
San Francisco, CA (United States)