FDA Import Refusal FR1-0012502-5/1/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0012502-5/1/1 from Nipro Corporation (Japan) on Dec 12, 2008. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charges: 341,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 12, 2008
Country
Japan
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
341,508

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