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FDA Import Refusal 110-9107818-8/1/1 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA refused shipment 110-9107818-8/1/1 from Cordis US Corp (United States) on February 6, 2006. The refused product falls under Devices — GUIDE, WIRE, CATHETER, NEUROVASCULATURE. Cited charges: 341,508

Refusal Details

Date
February 6, 2006
Country
United States
Product Category
Devices
Product Code
84MOF GUIDE, WIRE, CATHETER, NEUROVASCULATURE
Charges
341,508

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