FDA Import Refusal 799-7276157-0/11/1 — Acon Laboratories, Inc.

Acon Laboratories, Inc. — FEI 3003516723

The FDA refused shipment 799-7276157-0/11/1 from Acon Laboratories, Inc. (United States) on February 3, 2022. 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
February 3, 2022
Country
United States
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
508