FDA Import Refusal 8MA-0000945-9/12/1 — Shenzhen Kaiyan Medical Equipment Limited
The FDA refused shipment 8MA-0000945-9/12/1 from Shenzhen Kaiyan Medical Equipment Limited (China) on Oct 8, 2022. The refused product falls under Devices — OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE. Cited charge: 223 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Oct 8, 2022
- Country
- China
- Product Category
- Devices
- Product Code
- 79OLP OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
- Charges
- 223