FDA Import Refusal FR1-0019201-7/21/1 — NIPRO CORPORATION

NIPRO CORPORATION — FEI 3027266136

The FDA refused shipment FR1-0019201-7/21/1 from NIPRO CORPORATION (Japan) on May 8, 2025. 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
May 8, 2025
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.