FDA Import Refusal 799-7460751-8/12/1 — Guangzhou Pluslife Biotech Co., Ltd.

Guangzhou Pluslife Biotech Co., Ltd. — FEI 3037392657

The FDA refused shipment 799-7460751-8/12/1 from Guangzhou Pluslife Biotech Co., Ltd. (China) on Jun 13, 2025. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jun 13, 2025
Country
China
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
118,3280,508

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.