FDA Import Refusal 112-3610235-9/1/1 — Nipro Corporation

Nipro Corporation — FEI 3000247873

The FDA refused shipment 112-3610235-9/1/1 from Nipro Corporation (Japan) on Aug 5, 2008. The refused product falls under Devices — PHLEBOTOMY BLOOD COLLECTION KIT. Cited charges: 118,508 This firm has 5 or more other import refusals on record.