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FDA Import Refusal 112-2301185-5/4/1 — Admedes GmbH

Admedes GmbH — FEI 3003956144

The FDA refused shipment 112-2301185-5/4/1 from Admedes GmbH (Germany) on Apr 26, 2013. The refused product falls under Devices — PROSTHESIS, AORTIC VALVE, PERCUTANEOUSLY DELIVERED. Cited charges: 118,237 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 26, 2013
Country
Germany
Product Category
Devices
Product Code
74NPT PROSTHESIS, AORTIC VALVE, PERCUTANEOUSLY DELIVERED
Charges
118,237

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FDA data resources

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