Home / Import refusals / AL6-0051476-7/1/1

FDA Import Refusal AL6-0051476-7/1/1 — Beckman Coulter Inc.

Beckman Coulter Inc. — FEI 2050012

The FDA refused shipment AL6-0051476-7/1/1 from Beckman Coulter Inc. (United States) on January 17, 2012. The refused product falls under Devices — ACID, SODIUM HYALURONIC. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
January 17, 2012
Country
United States
Product Category
Devices
Product Code
75LZX ACID, SODIUM HYALURONIC
Charges
118,341

Recent inspections

  • 1149891 (NAI Thu Aug 05 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111029 (NAI Wed Oct 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791139 (NAI Mon Jul 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 725062 (OAI Thu May 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710437 (VAI Tue Feb 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • AEK-4315893-7/11/1 (Wed Mar 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 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)
  • 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