FDA Import Refusal 799-2074426-3/11/1 — NIPRO CANADA CORPORATION
The FDA refused shipment 799-2074426-3/11/1 from NIPRO CANADA CORPORATION (Canada) on Aug 2, 2019. The refused product falls under Devices — CATHETER, HEMODIALYSIS, IMPLANTED. Cited charges: 118,2780 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 2, 2019
- Country
- Canada
- Product Category
- Devices
- Product Code
- 78MSD CATHETER, HEMODIALYSIS, IMPLANTED
- Charges
- 118,2780