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FDA Import Refusal AEK-0010235-7/1/1 — PFM Medical Mepro GMBH

PFM Medical Mepro GMBH — FEI 3005704822

The FDA refused shipment AEK-0010235-7/1/1 from PFM Medical Mepro GMBH (Germany) on Jun 25, 2014. The refused product falls under Devices — DEVICE, TRANSCATHETER CARDIAC OCCLUSION. Cited charges: 118,237 This firm has 1 other import refusal on record.

Refusal Details

Date
Jun 25, 2014
Country
Germany
Product Category
Devices
Product Code
74MLV DEVICE, TRANSCATHETER CARDIAC OCCLUSION
Charges
118,237

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FDA data resources

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