FDA Import Refusal 231-0781160-0/1/1 — CareFusion DR 203 LTD

CareFusion DR 203 LTD — FEI 3007019930

The FDA refused shipment 231-0781160-0/1/1 from CareFusion DR 203 LTD (Dominican Republic) on July 26, 2011. The refused product falls under Devices — INSTRUMENT, BIOPSY. Cited charge: 508 This firm has 3 other import refusals on record.

Refusal Details

Date
July 26, 2011
Country
Dominican Republic
Product Category
Devices
Product Code
78KNW INSTRUMENT, BIOPSY
Charges
508