FDA Import Refusal 112-8624214-9/1/1 — Hemoteq AG

Hemoteq AG — FEI 3005969022

The FDA refused shipment 112-8624214-9/1/1 from Hemoteq AG (Germany) on Sep 7, 2012. The refused product falls under Devices — STENT, CARDIOVASCULAR. Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal details

Date
Sep 7, 2012
Country
Germany
Product Category
Devices
Product Code
74MAF STENT, CARDIOVASCULAR
Charges
237

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