FDA Warning Letter — Huestis Machine Corporation

Case 398551 — FEI 1219183

The FDA took a Warning Letter action against Huestis Machine Corporation on August 6, 2013 (Bristol, RI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Huestis Machine Corporation
Date
August 6, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Bristol, RI (United States)