FDA Import Refusal FR1-0018626-6/21/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0018626-6/21/1 from Nipro Corporation (Japan) on Oct 19, 2022. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Oct 19, 2022
Country
Japan
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
118

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