FDA Import Refusal AEK-8421560-5/11/1 — LYSIS HEALTHCARE GMBH

LYSIS HEALTHCARE GMBH — FEI 3015581439

The FDA refused shipment AEK-8421560-5/11/1 from LYSIS HEALTHCARE GMBH (Austria) on Apr 29, 2025. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,3280

Refusal Details

Date
Apr 29, 2025
Country
Austria
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,3280

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