FDA Warning Letter — Brymill Corporation

Case 46378 — FEI 1216795

The FDA took a Warning Letter action against Brymill Corporation on February 18, 2009 (Ellington, CT). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Brymill Corporation
Date
February 18, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Ellington, CT (United States)