FDA Import Refusal FR1-0012543-9/1/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0012543-9/1/1 from Nipro Corporation (Japan) on Jan 26, 2009. The refused product falls under Devices — DIALYZER, CAPILLARY, HOLLOW FIBER. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 26, 2009
Country
Japan
Product Category
Devices
Product Code
78FJI DIALYZER, CAPILLARY, HOLLOW FIBER
Charges
118

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