FDA Import Refusal 799-6702086-2/1/1 — Hemoteq AG

Hemoteq AG — FEI 3005969022

The FDA refused shipment 799-6702086-2/1/1 from Hemoteq AG (Germany) on Dec 9, 2014. The refused product falls under Devices — STENT, CARDIOVASCULAR. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 9, 2014
Country
Germany
Product Category
Devices
Product Code
74MAF STENT, CARDIOVASCULAR
Charges
508

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