Home / Import refusals / 224-0333936-3/1/8

FDA Import Refusal 224-0333936-3/1/8 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA refused shipment 224-0333936-3/1/8 from Terumo Medical Corporation (United States) on May 1, 2003. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 1, 2003
Country
United States
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,341

Recent inspections

  • 1317212 (NAI Fri May 01 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1182280 (NAI Fri Oct 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094113 (VAI Thu Jun 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003680 (VAI Fri Jan 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950051 (OAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 110-2383619-4/1/1V (Mon Oct 24 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 224-0333936-3/1/7 (Thu May 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 224-0332086-8/1/8 (Mon Mar 31 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 224-0332033-0/1/8 (Mon Mar 31 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 224-0332033-0/1/7 (Mon Mar 31 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources