FDA Import Refusal AEK-3621937-3/11/1 — DreamCon Co. Ltd.

DreamCon Co. Ltd. — FEI 3010460316

The FDA refused shipment AEK-3621937-3/11/1 from DreamCon Co. Ltd. (South Korea) on Jul 19, 2017. 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
Jul 19, 2017
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.