FDA Warning Letter — Kootenai Medical Center IRB

Case 407797 — FEI 1000221847

The FDA took a Warning Letter action against Kootenai Medical Center IRB on November 15, 2013 (Coeur d Alene, ID). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Kootenai Medical Center IRB
Date
November 15, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Coeur d Alene, ID (United States)