FDA Import Refusal 004-5998192-4/12/1 — Medtronic Inc

Medtronic Inc — FEI 2183870

The FDA refused shipment 004-5998192-4/12/1 from Medtronic Inc (United States) on Aug 10, 2011. The refused product falls under Devices — DEVICE, CORONARY SAPHENOUS VEIN BYPASS GRAFT, TEMPORARY, FOR EMBOLIZATION PROTECTION. Cited charge: 508 This firm has 5 or more other import refusals on record.