FDA Warning Letter — Hyperion Medical Technologies Inc

Case 411723 — FEI 3007674911

The FDA took a Warning Letter action against Hyperion Medical Technologies Inc on November 20, 2013 (Addison, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Hyperion Medical Technologies Inc
Date
November 20, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Addison, TX (United States)