FDA Warning Letter — Hsmg, Inc. D/b/a Smartinfuser Usa

Case 103567 — FEI 3004960040

The FDA took a Warning Letter action against Hsmg, Inc. D/b/a Smartinfuser Usa on July 29, 2010 (Houston, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Hsmg, Inc. D/b/a Smartinfuser Usa
Date
July 29, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Houston, TX (United States)