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FDA Import Refusal FR1-0016600-3/1/1 — Miyuki Elex Co.,Ltd

Miyuki Elex Co.,Ltd — FEI 3007482089

The FDA refused shipment FR1-0016600-3/1/1 from Miyuki Elex Co.,Ltd (Japan) on Dec 21, 2016. The refused product falls under Devices — DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 21, 2016
Country
Japan
Product Category
Devices
Product Code
78KDI DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
Charges
341

Other import refusals

FDA data resources

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