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FDA Import Refusal MH9-2048123-0/1/1 — Daiwha Corporation, Ltd

Daiwha Corporation, Ltd — FEI 3004448018

The FDA refused shipment MH9-2048123-0/1/1 from Daiwha Corporation, Ltd (South Korea) on Dec 11, 2015. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 11, 2015
Country
South Korea
Product Category
Devices
Product Code
79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Charges
118,341

Other import refusals

FDA data resources

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