FDA Import Refusal AEK-9210451-0/10003/1 — Guangzhou Pluslife Biotech Co., Ltd.
The FDA refused shipment AEK-9210451-0/10003/1 from Guangzhou Pluslife Biotech Co., Ltd. (China) on Jan 22, 2026. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jan 22, 2026
- Country
- China
- Product Category
- Devices
- Product Code
- 83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
- Charges
- 118,3280,508