FDA Warning Letter — R82 A/S

Case 412111 — FEI 3001657382

The FDA took a Warning Letter action against R82 A/S on October 18, 2013 (Gedved, Denmark). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
R82 A/S
Date
October 18, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Gedved (Denmark)