FDA Import Refusal 799-7481385-0/13/1 — BEIJING HOTGEN BIOTECH CO LTD
The FDA refused shipment 799-7481385-0/13/1 from BEIJING HOTGEN BIOTECH CO LTD (China) on May 28, 2025. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- May 28, 2025
- Country
- China
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 508