FDA Import Refusal AEK-7603992-2/10002/1 — MEDAX S.R.L. UNIPERSONALE
The FDA refused shipment AEK-7603992-2/10002/1 from MEDAX S.R.L. UNIPERSONALE (Italy) on Oct 22, 2025. The refused product falls under Devices — NEEDLE, SUTURING, DISPOSABLE. Cited charge: 16
Refusal Details
- Date
- Oct 22, 2025
- Country
- Italy
- Product Category
- Devices
- Product Code
- 79GAB NEEDLE, SUTURING, DISPOSABLE
- Charges
- 16