FDA Import Refusal FR1-0016883-5/11/1 — Miyuki Elex Co.,Ltd
The FDA refused shipment FR1-0016883-5/11/1 from Miyuki Elex Co.,Ltd (Japan) on Apr 3, 2017. The refused product falls under Devices — DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER). Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Apr 3, 2017
- Country
- Japan
- Product Category
- Devices
- Product Code
- 78KPO DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER)
- Charges
- 118,3280