FDA Warning Letter — Usine Rotec Inc

Case 385398 — FEI 3001752600

The FDA took a Warning Letter action against Usine Rotec Inc on January 7, 2013 (Baie-du-febvre, Canada). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Usine Rotec Inc
Date
January 7, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Baie-du-febvre (Canada)