Home / Import refusals / 112-1619008-2/1/1

FDA Import Refusal 112-1619008-2/1/1 — Bricon Technology GmbH

Bricon Technology GmbH — FEI 3004072627

The FDA refused shipment 112-1619008-2/1/1 from Bricon Technology GmbH (Germany) on November 21, 2003. The refused product falls under Devices — SPINAL VERTEBRAL BODY REPLACEMENT DEVICE. Cited charge: 226 This firm has 4 other import refusals on record.

Refusal Details

Date
November 21, 2003
Country
Germany
Product Category
Devices
Product Code
87MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
Charges
226

Recent inspections

  • 1109312 (NAI Thu Oct 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003949 (NAI Thu Feb 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867227 (VAI Thu Feb 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 112-2085195-2/1/1 (Tue Jul 11 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-8567663-1/1/1 (Mon Oct 24 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-4572587-4/1/1 (Thu Nov 18 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-4185683-0/1/1 (Thu Oct 14 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

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