FDA Warning Letter — DNA Genotek Inc.

Case 416225 — FEI 3003742580

The FDA took a Warning Letter action against DNA Genotek Inc. on December 20, 2013 (Kanata, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
DNA Genotek Inc.
Date
December 20, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Kanata (Canada)