Home / Import refusals / 98F-0091831-6/11/1

FDA Import Refusal 98F-0091831-6/11/1 — Becton Dickinson And Company

Becton Dickinson And Company — FEI 1911916

The FDA refused shipment 98F-0091831-6/11/1 from Becton Dickinson And Company (United States) on February 29, 2024. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
February 29, 2024
Country
United States
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
341

Recent inspections

  • 1012404 (VAI Fri May 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 985379 (VAI Thu Aug 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847638 (NAI Wed Sep 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 723716 (VAI Thu Apr 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 607365 (VAI Thu Aug 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-6704563-2/20002/1 (Mon Jun 01 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2232978-6/60001/1 (Thu Oct 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 98F-0109418-2/11/2 (Thu May 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9072913-2/11/1 (Tue May 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9637208-5/11/1A (Fri May 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources