FDA Import Refusal 799-0126122-2/11/1 — Hi-Lex Corporation
The FDA refused shipment 799-0126122-2/11/1 from Hi-Lex Corporation (Japan) on Aug 16, 2022. The refused product falls under Devices — CATHETER, PERCUTANEOUS. Cited charges: 118,3280,508
Refusal details
- Date
- Aug 16, 2022
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74DQY CATHETER, PERCUTANEOUS
- Charges
- 118,3280,508