FDA Import Refusal AEK-5376208-1/11/1 — SENBITEC
The FDA refused shipment AEK-5376208-1/11/1 from SENBITEC (South Korea) on Nov 30, 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
- Nov 30, 2018
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79OLP OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
- Charges
- 118,3280,508