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FDA Import Refusal 112-7996364-2/1/1 — Abiomed Europe GmbH

Abiomed Europe GmbH — FEI 3007904765

The FDA refused shipment 112-7996364-2/1/1 from Abiomed Europe GmbH (Germany) on October 14, 2010. The refused product falls under Devices — PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE. Cited charge: 118 This firm has 4 other import refusals on record.

Refusal Details

Date
October 14, 2010
Country
Germany
Product Category
Devices
Product Code
74KFM PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE
Charges
118

Recent inspections

  • 1194249 (NAI Thu Nov 10 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979231 (NAI Thu Jun 23 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 910065 (NAI Thu Dec 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-7973240-1/11/1 (Mon Dec 04 2023 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