FDA Warning Letter — CURALLUX LLC

Case 406944 — FEI 3010123655

The FDA took a Warning Letter action against CURALLUX LLC on September 20, 2013 (Doral, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
CURALLUX LLC
Date
September 20, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Doral, FL (United States)