Home / Import refusals / FR1-0019245-4/10002/2

FDA Import Refusal FR1-0019245-4/10002/2 — Goodman Co., Ltd

Goodman Co., Ltd — FEI 3007835716

The FDA refused shipment FR1-0019245-4/10002/2 from Goodman Co., Ltd (Japan) on August 19, 2025. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
August 19, 2025
Country
Japan
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
118,3280

Recent inspections

  • 1269122 (NAI Thu Apr 03 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1227869 (VAI Thu Jan 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • FR1-0019245-4/10002/1 (Tue Aug 19 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019201-7/11/1 (Thu May 08 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019201-7/31/1 (Thu May 08 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018965-8/11/1 (Thu Mar 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018965-8/21/1 (Thu Mar 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources