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FDA Import Refusal AEK-0364235-1/10002/1A — Kolmar Korea Co., Ltd. - Gwanjeong Factory

Kolmar Korea Co., Ltd. - Gwanjeong Factory — FEI 3010299845

The FDA refused shipment AEK-0364235-1/10002/1A from Kolmar Korea Co., Ltd. - Gwanjeong Factory (South Korea) on July 2, 2026. The refused product falls under Drugs and Biologics — ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.. Cited charges: 336,473 This firm has 5 or more other import refusals on record.

Refusal Details

Date
July 2, 2026
Country
South Korea
Product Category
Drugs and Biologics
Product Code
66PBY99 ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
Charges
336,473

Recent inspections

  • 1230224 (VAI Fri Feb 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1173870 (VAI Thu Jul 07 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1031995 (VAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-0644053-0/10002/2B (Thu Apr 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-0644053-0/10002/2A (Thu Apr 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-0279364-1/30003/1 (Fri Mar 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-0279364-1/40003/1 (Fri Mar 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7727435-3/10002/1 (Mon Nov 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources