FDA Import Refusal 799-3064398-7/11/2 — NIPRO CANADA CORPORATION

NIPRO CANADA CORPORATION — FEI 3005612924

The FDA refused shipment 799-3064398-7/11/2 from NIPRO CANADA CORPORATION (Canada) on Sep 10, 2024. The refused product falls under Devices — CATHETER, HEMODIALYSIS, IMPLANTED. Cited charge: 2780 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Sep 10, 2024
Country
Canada
Product Category
Devices
Product Code
78MSD CATHETER, HEMODIALYSIS, IMPLANTED
Charges
2780

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