FDA Warning Letter — BRI Institutional Review Board, Inc.

Case 70824 — FEI 1000220451

The FDA took a Warning Letter action against BRI Institutional Review Board, Inc. on October 5, 2009 (Houston, TX). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
BRI Institutional Review Board, Inc.
Date
October 5, 2009
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Houston, TX (United States)