FDA Import Refusal FR1-0016520-3/1/1 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA refused shipment FR1-0016520-3/1/1 from NIPRO CORP. (Japan) on Jul 11, 2016. The refused product falls under Devices — DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER). Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 11, 2016
Country
Japan
Product Category
Devices
Product Code
78KPO DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER)
Charges
118

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