FDA Import Refusal 799-7240804-2/12/1 — PLUSLIFE

PLUSLIFE — FEI 3036489724

The FDA refused shipment 799-7240804-2/12/1 from PLUSLIFE (China) on May 5, 2025. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,3280,508 This firm has 3 other import refusals on record.

Refusal Details

Date
May 5, 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.