FDA Import Refusal AEK-2413455-1/11/1 — DreamCon Co. Ltd.

DreamCon Co. Ltd. — FEI 3010460316

The FDA refused shipment AEK-2413455-1/11/1 from DreamCon Co. Ltd. (South Korea) on Nov 25, 2022. The refused product falls under Devices — LENS, CONTACT (OTHER MATERIAL) - DAILY. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Nov 25, 2022
Country
South Korea
Product Category
Devices
Product Code
86HQD LENS, CONTACT (OTHER MATERIAL) - DAILY
Charges
508

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