Home / Import refusals / 799-7973240-1/11/1

FDA Import Refusal 799-7973240-1/11/1 — Abiomed Europe GmbH

Abiomed Europe GmbH — FEI 3007904765

The FDA refused shipment 799-7973240-1/11/1 from Abiomed Europe GmbH (Germany) on December 4, 2023. The refused product falls under Devices — CONTROL, PUMP SPEED, CARDIOPULMONARY BYPASS. Cited charges: 118,508 This firm has 4 other import refusals on record.

Refusal Details

Date
December 4, 2023
Country
Germany
Product Category
Devices
Product Code
74DWA CONTROL, PUMP SPEED, CARDIOPULMONARY BYPASS
Charges
118,508

Recent inspections

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  • 910065 (NAI Thu Dec 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 112-7996364-2/1/1 (Thu Oct 14 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-6652000-8/1/1 (Thu Jun 21 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-6652000-8/1/2 (Thu Jun 21 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-6652000-8/2/1 (Thu Jun 21 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources