FDA Import Refusal AEK-5206620-3/11/1 — Hes Kwang Sun Enterprise
The FDA refused shipment AEK-5206620-3/11/1 from Hes Kwang Sun Enterprise (Taiwan) on Oct 12, 2018. The refused product falls under Devices — OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE. Cited charges: 118,3280,508
Refusal details
- Date
- Oct 12, 2018
- Country
- Taiwan
- Product Category
- Devices
- Product Code
- 79OLP OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
- Charges
- 118,3280,508