Home / Import refusals / AEK-0742586-0/10002/1

FDA Import Refusal AEK-0742586-0/10002/1 — DXM CO LTD

DXM CO LTD — FEI 3027302877

The FDA refused shipment AEK-0742586-0/10002/1 from DXM CO LTD (South Korea) on June 12, 2026. The refused product falls under Devices — ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
June 12, 2026
Country
South Korea
Product Category
Devices
Product Code
76EBZ ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION
Charges
118

Other import refusals

  • AYU-1009123-7/8/1 (Mon Jun 26 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AYU-1009123-7/6/1 (Mon Jun 26 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AYU-1009123-7/7/1 (Mon Jun 26 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AYU-1009123-7/9/1 (Mon Jun 26 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AYU-1009123-7/5/1 (Mon Jun 26 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources