FDA Import Refusal 799-1147132-6/10001/1 — Artivion, Inc

Artivion, Inc — FEI 3001451326

The FDA refused shipment 799-1147132-6/10001/1 from Artivion, Inc (United States) on September 4, 2025. The refused product falls under Devices — SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT. Cited charges: 118,237,3280 This firm has 1 other import refusal on record.