FDA Import Refusal AEK-9844848-1/10002/1 — NEUROVALENS LTD

NEUROVALENS LTD — FEI 3027997270

The FDA refused shipment AEK-9844848-1/10002/1 from NEUROVALENS LTD (United Kingdom) on Sep 11, 2026. The refused product falls under Devices — CRANIAL ELECTROTHERAPY STIMULATOR TO TREAT DEPRESSION. Cited charge: 3280 This firm has 2 other import refusals on record.

Refusal Details

Date
Sep 11, 2026
Country
United Kingdom
Product Category
Devices
Product Code
84JXK CRANIAL ELECTROTHERAPY STIMULATOR TO TREAT DEPRESSION
Charges
3280

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