FDA Import Refusal AEK-5134835-5/11/1 — Danalife ApS
The FDA refused shipment AEK-5134835-5/11/1 from Danalife ApS (Denmark) on May 22, 2024. The refused product falls under Devices — DEVICE, EXTERNAL PENILE RIGIDITY. Cited charge: 508 This firm has 4 other import refusals on record.
Refusal Details
- Date
- May 22, 2024
- Country
- Denmark
- Product Category
- Devices
- Product Code
- 78LKY DEVICE, EXTERNAL PENILE RIGIDITY
- Charges
- 508