FDA Import Refusal 231-8522860-3/31/1 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA refused shipment 231-8522860-3/31/1 from NIPRO CORP. (Japan) on Jan 14, 2020. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charge: 479 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 14, 2020
Country
Japan
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
479

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