BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Fastep COVID-19 Antigen Home Test

    Reg #: 3031161873 · FEI: 3031161873 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    AFTON DX LLC
    Registration Number
    3031161873
    FEI Number
    3031161873
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1773 Wright Avenue
    City
    La Verne
    State
    CA
    ZIP
    91750
    Country
    US

    Owner / Operator

    Firm Name
    Afton Dx LLC
    Operator Number
    10090792
    Address
    1773 Wright Avenue
    City
    La Verne
    State
    CA
    Postal Code
    91750
    Country
    US
    Correspondent
    Jason Wang

    Products

    Device Name Product Code
    Coronavirus Antigen Detection Test System. QKP

    Proprietary Names

    Fastep COVID-19 Antigen Home Test

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)