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FDA Import Refusal M21-0759246-3/22/1 — Metrax Gmbh

Metrax Gmbh — FEI 3001417379

The FDA refused shipment M21-0759246-3/22/1 from Metrax Gmbh (Germany) on Jul 17, 2019. The refused product falls under Devices — DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATION. Cited charges: 118,3280,341,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 17, 2019
Country
Germany
Product Category
Devices
Product Code
74NIK DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATION
Charges
118,3280,341,508

Other import refusals

FDA data resources

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