Home / Import refusals / AEK-6441026-6/31/1

FDA Import Refusal AEK-6441026-6/31/1 — Bausch & Lomb Inc

Bausch & Lomb Inc — FEI 1920664

The FDA refused shipment AEK-6441026-6/31/1 from Bausch & Lomb Inc (United States) on November 26, 2019. The refused product falls under Devices — UNIT, PHACOFRAGMENTATION. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 26, 2019
Country
United States
Product Category
Devices
Product Code
86HQC UNIT, PHACOFRAGMENTATION
Charges
341

Recent inspections

  • 1107226 (NAI Tue Oct 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 978030 (NAI Fri Jun 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 826558 (NAI Fri Mar 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 784537 (NAI Fri Jun 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 782300 (VAI Thu May 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-7030224-4/30002/1 (Mon Jun 01 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-7293114-8/11/1 (Mon Oct 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 605-6602753-2/21/1 (Wed Sep 02 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 508-0386653-7/11/1 (Fri Feb 28 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 267-0197695-8/661/1 (Tue Jul 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources