FDA Warning Letter — ARxIUM Inc.

Case 262774 — FEI 3006227536

The FDA took a Warning Letter action against ARxIUM Inc. on February 8, 2012 (Winnipeg, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
ARxIUM Inc.
Date
February 8, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Winnipeg (Canada)