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FDA Import Refusal FR1-0017092-2/11/2 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA refused shipment FR1-0017092-2/11/2 from NIPRO CORP. (Japan) on Dec 8, 2017. The refused product falls under Devices — CATHETER, RETENTION TYPE, BALLOON. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 8, 2017
Country
Japan
Product Category
Devices
Product Code
78EZL CATHETER, RETENTION TYPE, BALLOON
Charges
118

Recent inspections

Other import refusals

FDA data resources

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