FDA Import Refusal FR1-0011955-6/1/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0011955-6/1/1 from Nipro Corporation (Japan) on Oct 1, 2007. The refused product falls under Devices — NEEDLE, SPINAL, SHORT TERM. Cited charge: 476 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 1, 2007
Country
Japan
Product Category
Devices
Product Code
80MIA NEEDLE, SPINAL, SHORT TERM
Charges
476

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