Home / Import refusals / AEK-4315893-7/11/1

FDA Import Refusal AEK-4315893-7/11/1 — Beckman Coulter Gmbh

Beckman Coulter Gmbh — FEI 3002721051

The FDA refused shipment AEK-4315893-7/11/1 from Beckman Coulter Gmbh (Germany) on March 21, 2018. The refused product falls under Devices — RESEARCH USE ONLY/HEMATOLOGY DEVICES. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 21, 2018
Country
Germany
Product Category
Devices
Product Code
81OTQ RESEARCH USE ONLY/HEMATOLOGY DEVICES
Charges
118,3280

Other import refusals

  • 799-7704964-7/1/1 (Thu Nov 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • F23-0764273-6/1/1 (Thu Feb 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AL6-0051476-7/1/1 (Tue Jan 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 322-0303175-6/1/1 (Mon Aug 09 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • EE6-2008272-1/1/1 (Wed Jul 16 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources