FDA Import Refusal 799-6512456-1/31/1 — KANEKA MEDIX CORPORATION KANAGAWA PLANT
The FDA refused shipment 799-6512456-1/31/1 from KANEKA MEDIX CORPORATION KANAGAWA PLANT (Japan) on Apr 17, 2020. The refused product falls under Devices — CATHETER, PERCUTANEOUS. Cited charge: 118
Refusal details
- Date
- Apr 17, 2020
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74DQY CATHETER, PERCUTANEOUS
- Charges
- 118