FDA Warning Letter — Batrik Medical Mfg., Inc.

Case 410595 — FEI 3003749234

The FDA took a Warning Letter action against Batrik Medical Mfg., Inc. on September 23, 2013 (Lachine, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Batrik Medical Mfg., Inc.
Date
September 23, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Lachine (Canada)