FDA Inspection 821084 — Techlem Medical Corporation

Techlem Medical Corporation — FEI 3000134760

The FDA completed an inspection of Techlem Medical Corporation on Feb 28, 2013 in Mississauga. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mississauga (Canada)

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