FDA Warning Letter — Rehabtronics Inc.

Case 415125 — FEI 3007999109

The FDA took a Warning Letter action against Rehabtronics Inc. on December 4, 2013 (Edmonton, Canada). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Rehabtronics Inc.
Date
December 4, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Edmonton (Canada)