FDA Import Refusal 799-1147132-6/10001/1 — Artivion, Inc
The FDA refused shipment 799-1147132-6/10001/1 from Artivion, Inc (United States) on Sep 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.
Refusal Details
- Date
- Sep 4, 2025
- Country
- United States
- Product Category
- Devices
- Product Code
- 74MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Charges
- 118,237,3280