FDA Import Refusal MT3-0111645-5/1/1 — Sungyong Meditech

Sungyong Meditech — FEI 3009791902

The FDA refused shipment MT3-0111645-5/1/1 from Sungyong Meditech (South Korea) on Nov 25, 2015. The refused product falls under Devices — SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC. Cited charges: 118,3280,341

Refusal details

Date
Nov 25, 2015
Country
South Korea
Product Category
Devices
Product Code
90IYO SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
Charges
118,3280,341

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