FDA Import Refusal 8K4-0072145-0/41/1 — Ashitaka Factory Of Terumo Corporation
The FDA refused shipment 8K4-0072145-0/41/1 from Ashitaka Factory Of Terumo Corporation (Japan) on Apr 8, 2025. The refused product falls under Devices — CATHETER, PERCUTANEOUS. Cited charge: 3280
Refusal Details
- Date
- Apr 8, 2025
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74DQY CATHETER, PERCUTANEOUS
- Charges
- 3280