FDA Import Refusal M50-0176040-9/1/1 — Techlem Medical Corporation

Techlem Medical Corporation — FEI 3000134760

The FDA refused shipment M50-0176040-9/1/1 from Techlem Medical Corporation (Canada) on Dec 13, 2011. The refused product falls under Devices — STRETCHER, WHEELED. Cited charge: 341 This firm has 1 other import refusal on record.

Refusal Details

Date
Dec 13, 2011
Country
Canada
Product Category
Devices
Product Code
80FPO STRETCHER, WHEELED
Charges
341

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