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

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.