FDA Import Refusal AEK-6009515-1/1/1 — Artivion, Inc

Artivion, Inc — FEI 3001451326

The FDA refused shipment AEK-6009515-1/1/1 from Artivion, Inc (United States) on March 19, 2004. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charges: 341,508 This firm has 1 other import refusal on record.