FDA Import Refusal AEK-9054152-2/11/1 — Rayence Co. Ltd.

Rayence Co. Ltd. — FEI 3009048384

The FDA refused shipment AEK-9054152-2/11/1 from Rayence Co. Ltd. (South Korea) on May 20, 2021. The refused product falls under Devices — SYSTEM, X-RAY, EXTRAORAL SOURCE, DIGITAL. Cited charges: 2480,341

Refusal details

Date
May 20, 2021
Country
South Korea
Product Category
Devices
Product Code
90MUH SYSTEM, X-RAY, EXTRAORAL SOURCE, DIGITAL
Charges
2480,341

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