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FDA Import Refusal AEK-9138778-5/10002/1 — Kolmar Korea Co., Ltd. Bucheon Factory

Kolmar Korea Co., Ltd. Bucheon Factory — FEI 3010818961

The FDA refused shipment AEK-9138778-5/10002/1 from Kolmar Korea Co., Ltd. Bucheon Factory (South Korea) on March 6, 2026. The refused product falls under Drugs and Biologics — HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN). Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 6, 2026
Country
South Korea
Product Category
Drugs and Biologics
Product Code
66PBJ05 HOMOSALATE (ULTRAVIOLET SCREEN/SUNSCREEN)
Charges
118,3280

Recent inspections

  • 1256315 (VAI Fri Dec 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1087335 (NAI Fri Mar 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-7736334-7/20002/1 (Mon Nov 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-1375271-4/11/1 (Wed Jul 24 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-4931235-2/71/1 (Tue Jul 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-4931235-2/81/1 (Tue Jul 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-4931235-2/91/1 (Tue Jul 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources