FDA Warning Letter — Techlem Medical Corporation

Case 395879 — FEI 3000134760

The FDA took a Warning Letter action against Techlem Medical Corporation on Jun 4, 2013 (Mississauga, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Techlem Medical Corporation
Date
Jun 4, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Mississauga (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.