FDA Warning Letter — Defibtech, LLC

Case 133290 — FEI 3003521780

The FDA took a Warning Letter action against Defibtech, LLC on September 22, 2010 (Guilford, CT). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Defibtech, LLC
Date
September 22, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Guilford, CT (United States)