FDA Import Refusal EQ6-0023210-0/11/1 — SYNTELLIX AG

SYNTELLIX AG — FEI 3013683185

The FDA refused shipment EQ6-0023210-0/11/1 from SYNTELLIX AG (Germany) on Oct 5, 2017. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charges: 118,3280,341

Refusal details

Date
Oct 5, 2017
Country
Germany
Product Category
Devices
Product Code
80LDQ DEVICE, GENERAL MEDICAL
Charges
118,3280,341

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