FDA Import Refusal 112-4344446-5/1/1 — NIPRO CANADA CORPORATION

NIPRO CANADA CORPORATION — FEI 3005612924

The FDA refused shipment 112-4344446-5/1/1 from NIPRO CANADA CORPORATION (Canada) on Dec 28, 2011. The refused product falls under Devices — CATHETER, HEMODIALYSIS, IMPLANTED. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Dec 28, 2011
Country
Canada
Product Category
Devices
Product Code
78MSD CATHETER, HEMODIALYSIS, IMPLANTED
Charges
341

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