Home / Import refusals / AEK-8086893-6/11/1

FDA Import Refusal AEK-8086893-6/11/1 — ALEXANDRA DUMITRU

ALEXANDRA DUMITRU — FEI 3033537384

The FDA refused shipment AEK-8086893-6/11/1 from ALEXANDRA DUMITRU (Ireland) on Dec 23, 2024. The refused product falls under Devices — AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE). Cited charges: 118,3280,341

Refusal Details

Date
Dec 23, 2024
Country
Ireland
Product Category
Devices
Product Code
74MKJ AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE)
Charges
118,3280,341

FDA data resources

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