See QR code instructions at end of report
Your test results were NEGATIVE for COVID-19.
Your full lab report is included with this letter and should be used as proof of your test result when such proof is requested.
We encourage you to contact your healthcare provider if you have any health concerns as a negative test result may rarely occur in patients with a COVID-19 infection. Please continue to take the necessary precautions including social distancing, hand hygiene, cough/sneeze etiquette, using a face cover and proper surface cleaning to keep yourself and others around you healthy. Sincerely,
Your Walgreens Pharmacy Team
To save your COVID-19 test results:
• Download and open a SMART Health Card-compatible app, such as CommonPass.
• Follow in-app instructions to save your COVID-19 test results. Link to CommonPass download: https://thecommonsproject.org/shc Customer Care: 1-800-WALGREENS www.walgreens.com Member of Walgreens Boots Alliance Jeanluke Ekmekjian
12310 BURBANK BLVD APT 10
VALLEY VILLAGE, CA 91607
18515 DEVONSHIRE ST
6347
Northridge, CA 91324
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Aegis Sciences Corporation
501 Great Circle Road
Nashville, TN 37228
Report To: Armaghan Azad
18515 DEVONSHIRE ST
NORTHRIDGE, CA 91324
Client: WALGREENS NORTHRIDGE 6347
Patient ID:
Lab Sample ID:
PATIENT:
Specimen Type:
Collected:
Reported:
813311510
Sample Information
Nasal - Anterior Nares
04/13/2022 16:00 Pacific Time
04/15/2022
Lab Director: Matthew T. Hardison, PhD
Client Information
Received: 04/14/2022
Jeanluke Ekmekjian
12310 BURBANK BLVD APT 10,
VALLEY VILLAGE CA, 91607
Los Angeles
Phone: 559-***-****
DOB: 05/17/2007
Gender: Male
Race: White
Laboratory Report CLIA#: 44D2062333
Visit https://www.aegislabs.com/our-services/covid19-testing for COVID-19 testing resources Test(s) Requested
05700 SARS-CoV-2, RT-PCR
Tested For Result Reference Range
SARS-CoV-2, RT-PCR
SARS-CoV-2 NEGATIVE N/A
The Thermo Fisher Scientific, Inc. TaqPath COVID-19 Combo Kit used to perform this test has been authorized by FDA under an Emergency Use Authorization for use by authorized laboratories. The test has not been otherwise FDA cleared or approved. This test is authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under section 564(b)(1) of the Act, 21 U.S.C. 360bbb-3(b)(1), unless the authorization is terminated or revoked. Lab Director: Matthew T. Hardison, PhD
4/15/2022 11:30:58 AM