FDA Warning Letter — Trinity Health Michigan Regional IRB #4

Case 398804 — FEI 1825380

The FDA took a Warning Letter action against Trinity Health Michigan Regional IRB #4 on Aug 1, 2013 (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
Aug 1, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Pontiac, MI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.