FDA Import Refusal AEK-0500310-6/11/1 — DreamCon Co. Ltd.

DreamCon Co. Ltd. — FEI 3010460316

The FDA refused shipment AEK-0500310-6/11/1 from DreamCon Co. Ltd. (South Korea) on Apr 5, 2022. The refused product falls under Devices — LENS, CONTACT (DISPOSABLE). Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 5, 2022
Country
South Korea
Product Category
Devices
Product Code
86MVN LENS, CONTACT (DISPOSABLE)
Charges
237

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