FDA Import Refusal K51-0073431-5/1/1 — Medtec

Medtec — FEI 3003058017

The FDA refused shipment K51-0073431-5/1/1 from Medtec (Germany) on Feb 13, 2012. The refused product falls under Devices — ASSEMBLY, TUBE HOUSING, X-RAY, DIAGNOSTIC. Cited charge: 118 This firm has 1 other import refusal on record.

Refusal details

Date
Feb 13, 2012
Country
Germany
Product Category
Devices
Product Code
90ITY ASSEMBLY, TUBE HOUSING, X-RAY, DIAGNOSTIC
Charges
118

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