FDA Import Refusal AEK-0253503-4/1/1 — Corentec Co., LTD

Corentec Co., LTD — FEI 3009106092

The FDA refused shipment AEK-0253503-4/1/1 from Corentec Co., LTD (South Korea) on Sep 25, 2014. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charge: 118

Refusal details

Date
Sep 25, 2014
Country
South Korea
Product Category
Devices
Product Code
80LDQ DEVICE, GENERAL MEDICAL
Charges
118

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