FDA Import Refusal FR1-0018848-6/21/1 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA refused shipment FR1-0018848-6/21/1 from NIPRO CORP. (Japan) on Jan 26, 2024. The refused product falls under Devices — OXYGENATOR, CARDIOPULMONARY BYPASS. Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 26, 2024
Country
Japan
Product Category
Devices
Product Code
74DTZ OXYGENATOR, CARDIOPULMONARY BYPASS
Charges
237

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