Home / Import refusals / 224-0360913-8/1/24

FDA Import Refusal 224-0360913-8/1/24 — Covidien LP

Covidien LP — FEI 1282497

The FDA refused shipment 224-0360913-8/1/24 from Covidien LP (United States) on May 23, 2008. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3340,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 23, 2008
Country
United States
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3340,508

Recent inspections

  • 1191674 (VAI Fri Nov 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 844859 (VAI Thu Aug 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 792561 (VAI Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 778312 (NAI Mon Apr 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 745728 (NAI Tue Sep 20 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • SCS-6646173-6/11/1 (Thu Nov 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2601515-8/21/1 (Mon Oct 07 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 231-7179998-0/11/1 (Thu Mar 09 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2389325-9/11/1 (Fri Dec 30 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-8430821-2/21/1 (Thu Jul 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources