Home / Import refusals / K51-0068523-6/2/1

FDA Import Refusal K51-0068523-6/2/1 — Vygon SA

Vygon SA — FEI 3009291251

The FDA refused shipment K51-0068523-6/2/1 from Vygon SA (France) on March 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
March 1, 2010
Country
France
Product Category
Devices
Product Code
80FOS CATHETER, UMBILICAL ARTERY
Charges
508

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Other import refusals

  • 799-0577988-4/1/1 (Tue Oct 29 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • K51-0069182-0/3/1 (Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • K51-0069182-0/2/1 (Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • K51-0069182-0/4/1 (Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • K51-0069182-0/1/1 (Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources