Home / Import refusals / AEK-6466891-2/2/1

FDA Import Refusal AEK-6466891-2/2/1 — Cantor & Barnard Ltd.

Cantor & Barnard Ltd. — FEI 3002807717

The FDA refused shipment AEK-6466891-2/2/1 from Cantor & Barnard Ltd. (United Kingdom) on November 19, 2004. The refused product falls under Devices — LENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 19, 2004
Country
United Kingdom
Product Category
Devices
Product Code
86NJH LENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT
Charges
118

Recent inspections

  • 1254939 (VAI Thu Nov 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1187279 (VAI Thu Nov 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 725036 (OAI Thu Apr 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 584984 (NAI Thu May 07 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 1FX-7374199-2/10002/1 (Tue Jun 23 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 1FX-7374199-2/20002/1 (Tue Jun 23 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-7050145-7/11/1 (Wed Mar 02 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-6592102-1/1/1 (Wed Aug 03 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-6581950-6/1/1 (Tue Aug 02 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources