FDA Import Refusal AEK-6817854-7/12/1 — SHENZHEN KAIYAN MEDICAL EQUIPMENT
The FDA refused shipment AEK-6817854-7/12/1 from SHENZHEN KAIYAN MEDICAL EQUIPMENT (China) on Feb 14, 2020. The refused product falls under Devices — OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE. Cited charge: 223 This firm has 1 other import refusal on record.
Refusal details
- Date
- Feb 14, 2020
- Country
- China
- Product Category
- Devices
- Product Code
- 79OLP OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
- Charges
- 223