FDA Import Refusal FR1-0016784-5/11/1 — Miyuki Elex Co.,Ltd

Miyuki Elex Co.,Ltd — FEI 3007482089

The FDA refused shipment FR1-0016784-5/11/1 from Miyuki Elex Co.,Ltd (Japan) on Jan 17, 2017. The refused product falls under Devices — DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER). Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 17, 2017
Country
Japan
Product Category
Devices
Product Code
78KPO DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER)
Charges
118,3280

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