Home / Import refusals / 799-7599984-0/10003/1

FDA Import Refusal 799-7599984-0/10003/1 — KDC/ONE Development Corporation, Inc.

KDC/ONE Development Corporation, Inc. — FEI 3003690512

The FDA refused shipment 799-7599984-0/10003/1 from KDC/ONE Development Corporation, Inc. (Canada) on November 21, 2025. The refused product falls under Drugs and Biologics — MENTHOL (ANTI-PRURITIC). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 21, 2025
Country
Canada
Product Category
Drugs and Biologics
Product Code
62MBQ08 MENTHOL (ANTI-PRURITIC)
Charges
75

Recent inspections

  • 1195720 (VAI Fri Jan 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1026564 (VAI Thu Sep 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 911255 (NAI Fri Oct 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 829358 (NAI Thu Dec 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 612357 (NAI Wed Aug 12 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-2341764-4/10002/1 (Wed May 20 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-6734385-4/10002/1 (Tue May 12 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-4622194-5/10003/1 (Mon Apr 20 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-3730175-0/10002/3 (Fri Apr 17 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • DN2-3015112-3/31/1 (Tue Feb 18 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources