FDA Warning Letter — Trinity Health Michigan Regional IRB #4

Case 470506 — FEI 1825380

The FDA took a Warning Letter action against Trinity Health Michigan Regional IRB #4 on September 15, 2015 (Pontiac, MI). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Trinity Health Michigan Regional IRB #4
Date
September 15, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Pontiac, MI (United States)