FDA Import Refusal AEK-4818222-2/11/1 — DEFIBSPLUS PTY LTD
The FDA refused shipment AEK-4818222-2/11/1 from DEFIBSPLUS PTY LTD (Australia) on Apr 1, 2024. The refused product falls under Devices — WEARABLE, DEFIBRILLATOR, AUTOMATIC, EXTERNAL. Cited charges: 118,237,3280
Refusal Details
- Date
- Apr 1, 2024
- Country
- Australia
- Product Category
- Devices
- Product Code
- 74MVK WEARABLE, DEFIBRILLATOR, AUTOMATIC, EXTERNAL
- Charges
- 118,237,3280