At home antigen test results are now accepted by the CDC from travelers who are returning to the United States. Only tests that have received an Emergency Use Authorization such as the Flowflex™ SARS-CoV-2 Antigen Rapid Test (self-test) can be used for this purpose. You must take your test under video observation with ID verification and receive a validated result. AZOVA will provide you with these services.
Purchase your test kit (if needed). Schedule your video observation call within the timeframe that you need to take your test. Schedule a separate appointment for each person who will be taking a test. All members of your group can join the call together, but each person must have their own appointment registration.
Note: If you are scheduling on behalf of a dependent, first create your own account and then add your dependent’s information on the screen where it asks who is the patient.
United States Requirement*
Get tested on | MON | TUE | WED | THU | FRI | SAT | SUN |
For results needed on | TUE | WED | THU | FRI | SAT | SUN | MON |
Get tested on | MON | TUE | WED | THU | FRI | SAT | SUN |
For results needed on | WED | THU | FRI | SAT | SUN | MON | TUE |
Get tested on | MON | TUE | WED | THU | FRI | SAT | SUN |
For results needed on | THU | FRI | SAT | SUN | MON | TUE | WED |
Get tested on | MON | TUE | WED | THU | FRI | SAT | SUN |
For results needed on | SAT | SUN | MON | TUE | WED | THU | FRI |
You can chat with AZOVA’s Customer Support team for comprehensive support, including help with your account, testing, shipping, and results. We typically respond within 3 minutes or less. Click the messaging icon on the lower right corner of the page to get started.
Talk with Customer Support
You can call the dedicated support line using the number below. Please note that wait times may vary depending on call volume.
(844) 692–9682This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA;
This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and,
The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
You can review the instructions for use here.
Fact Sheet for Healthcare Professionals.