Home / Import refusals / AEK-5091123-6/11/1

FDA Import Refusal AEK-5091123-6/11/1 — Bausch & Lomb, Inc.

Bausch & Lomb, Inc. — FEI 1000119305

The FDA refused shipment AEK-5091123-6/11/1 from Bausch & Lomb, Inc. (United States) on September 26, 2018. The refused product falls under Devices — KNIFE, OPHTHALMIC. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 26, 2018
Country
United States
Product Category
Devices
Product Code
86HNN KNIFE, OPHTHALMIC
Charges
118

Recent inspections

  • 1107243 (NAI Thu Oct 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 973794 (NAI Thu Jun 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876296 (NAI Mon Apr 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 766406 (NAI Thu Jan 19 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)
  • AEK-6441026-6/31/1 (Tue Nov 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources