FDA Import Refusal AEK-5229901-1/11/1 — NEUROVALENS LTD
The FDA refused shipment AEK-5229901-1/11/1 from NEUROVALENS LTD (United Kingdom) on May 31, 2024. The refused product falls under Devices — CRANIAL ELECTROTHERAPY STIMULATOR TO TREAT INSOMNIA AND/OR ANXIETY. Cited charges: 118,3280,341 This firm has 2 other import refusals on record.
Refusal Details
- Date
- May 31, 2024
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 84QJQ CRANIAL ELECTROTHERAPY STIMULATOR TO TREAT INSOMNIA AND/OR ANXIETY
- Charges
- 118,3280,341