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FDA Import Refusal FR1-0017338-9/11/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0017338-9/11/1 from Nipro Corporation (Japan) on Aug 22, 2018. The refused product falls under Devices — CATHETER, EMBOLECTOMY. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 22, 2018
Country
Japan
Product Category
Devices
Product Code
74DXE CATHETER, EMBOLECTOMY
Charges
118,3280

Other import refusals

FDA data resources

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