FDA Import Refusal 300-5581061-7/1/1 — Eurocor Gmbh

Eurocor Gmbh — FEI 3009339379

The FDA refused shipment 300-5581061-7/1/1 from Eurocor Gmbh (Germany) on Apr 3, 2019. The refused product falls under Devices — STENT, CARDIOVASCULAR. Cited charge: 118 This firm has 1 other import refusal on record.

Refusal details

Date
Apr 3, 2019
Country
Germany
Product Category
Devices
Product Code
74MAF STENT, CARDIOVASCULAR
Charges
118

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