FDA Import Refusal FR1-0011803-8/1/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment FR1-0011803-8/1/1 from Nipro Corporation (Japan) on May 29, 2007. The refused product falls under Devices — NEEDLE, SPINAL, SHORT TERM. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
May 29, 2007
Country
Japan
Product Category
Devices
Product Code
80MIA NEEDLE, SPINAL, SHORT TERM
Charges
508

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