FDA Warning Letter — ReliantHeart Inc.

Case 86444 — FEI 3003259341

The FDA took a Warning Letter action against ReliantHeart Inc. on December 15, 2009 (Houston, TX). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
ReliantHeart Inc.
Date
December 15, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Houston, TX (United States)