Home / Import refusals / 112-6652000-8/2/1

FDA Import Refusal 112-6652000-8/2/1 — Abiomed Europe GmbH

Abiomed Europe GmbH — FEI 3007904765

The FDA refused shipment 112-6652000-8/2/1 from Abiomed Europe GmbH (Germany) on June 21, 2007. The refused product falls under Devices — GUIDEWIRE, CATHETER, REPROCESSED. 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
74NKQ GUIDEWIRE, CATHETER, REPROCESSED
Charges
118,508

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)
  • 112-7996364-2/1/1 (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)

FDA data resources