FDA Import Refusal 510-7570801-9/1/1 — Avantec Vascular Corporation
The FDA refused shipment 510-7570801-9/1/1 from Avantec Vascular Corporation (United States) on June 24, 2005. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charge: 237 This firm has 2 other import refusals on record.
Refusal Details
- Date
- June 24, 2005
- Country
- United States
- Product Category
- Devices
- Product Code
- 74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
- Charges
- 237