FDA Import Refusal AEK-0581059-2/10002/1 — GEOTEK MEDIKAL VE SAGLIK HIZ.TIC.SA

GEOTEK MEDIKAL VE SAGLIK HIZ.TIC.SA — FEI 3029668289

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.