FDA Import Refusal 510-1135572-7/1/1 — Asahi Kasei Pharma Corporation Diagnostics Dept.
The FDA refused shipment 510-1135572-7/1/1 from Asahi Kasei Pharma Corporation Diagnostics Dept. (Japan) on Dec 13, 2010. The refused product falls under Devices — DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM. Cited charges: 118,341,508
Refusal details
- Date
- Dec 13, 2010
- Country
- Japan
- Product Category
- Devices
- Product Code
- 78KDI DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
- Charges
- 118,341,508