FDA Warning Letter — Refine USA, LLC

Case 90984 — FEI 3006033709

The FDA took a Warning Letter action against Refine USA, LLC on April 18, 2011 (Jacksonville, FL). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Refine USA, LLC
Date
April 18, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Jacksonville, FL (United States)