FDA Import Refusal AEK-0581059-2/10002/1 — GEOTEK MEDIKAL VE SAGLIK HIZ.TIC.SA
The FDA refused shipment AEK-0581059-2/10002/1 from GEOTEK MEDIKAL VE SAGLIK HIZ.TIC.SA (Turkey) on Jul 24, 2026. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charge: 3904
Refusal Details
- Date
- Jul 24, 2026
- Country
- Turkey
- Product Category
- Devices
- Product Code
- 90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
- Charges
- 3904