FDA Import Refusal K51-0068523-6/3/1 — Vygon SA
The FDA refused shipment K51-0068523-6/3/1 from Vygon SA (France) on Mar 1, 2010. The refused product falls under Devices — CATHETER, UMBILICAL ARTERY. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Mar 1, 2010
- Country
- France
- Product Category
- Devices
- Product Code
- 80FOS CATHETER, UMBILICAL ARTERY
- Charges
- 508