FDA Import Refusal AEK-5653886-9/11/1 — Sonoscape America Inc
The FDA refused shipment AEK-5653886-9/11/1 from Sonoscape America Inc (United States) on Aug 30, 2024. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,3280,341
Refusal Details
- Date
- Aug 30, 2024
- Country
- United States
- Product Category
- Devices
- Product Code
- 90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
- Charges
- 118,3280,341