FDA Import Refusal AEK-5510870-6/11/1 — DX PRODUCTS LIMITED
The FDA refused shipment AEK-5510870-6/11/1 from DX PRODUCTS LIMITED (United Kingdom) on Jul 25, 2024. The refused product falls under Devices — DEVICE, EXTERNAL PENILE RIGIDITY. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jul 25, 2024
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 78LKY DEVICE, EXTERNAL PENILE RIGIDITY
- Charges
- 341