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FDA Import Refusal 112-6652000-8/1/1 — Abiomed Europe GmbH

Abiomed Europe GmbH — FEI 3007904765

The FDA refused shipment 112-6652000-8/1/1 from Abiomed Europe GmbH (Germany) on June 21, 2007. The refused product falls under Devices — PUMP BLOOD, CARDIOPULMONARY BYPASS, ROLLER TYPE. Cited charges: 118,508 This firm has 4 other import refusals on record.

Refusal Details

Date
June 21, 2007
Country
Germany
Product Category
Devices
Product Code
74DWB PUMP BLOOD, CARDIOPULMONARY BYPASS, ROLLER TYPE
Charges
118,508

Recent inspections

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Other import refusals

  • 799-7973240-1/11/1 (Mon Dec 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-7996364-2/1/1 (Thu Oct 14 2010 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)

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