FDA Import Refusal AEK-5002656-4/11/1 — Cardicare Company, LTD
The FDA refused shipment AEK-5002656-4/11/1 from Cardicare Company, LTD (China) on Apr 24, 2024. The refused product falls under Devices — CUFF, BLOOD-PRESSURE. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Apr 24, 2024
- Country
- China
- Product Category
- Devices
- Product Code
- 74DXQ CUFF, BLOOD-PRESSURE
- Charges
- 508