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WARNING LETTER
•Avazo-Healthcare, LLC•November 16, 2020

Avazo-Healthcare, LLC – FDA Warning Letter, Nov 16, 2020

Record Details

On November 30, 2020, the FDA issued a Warning Letter to CBD Market Web and COVID Test Shop, located at 605 Louis Dr Ste 502, Warminster, PA 18974. The letter addresses violations observed on their websites, https://www.covidtests.shop and www.cbdmarketweb.com, and associated social media pages, from August 21, 2020, through November 16, 2020.

The FDA found that the companies were selling unapproved and unauthorized COVID-19 test kits and CBD products with claims to mitigate, prevent, treat, diagnose, or cure COVID-19. Specifically, the "COVID-19 Ag Rapid Test Cassette" and "COVID-19 Coronavirus Spike Glycoprotein Antigen Ag Rapid Test Kit" were deemed adulterated under 21 U.S.C. § 351(f)(1)(B) and misbranded under 21 U.S.C. § 352(o) because they lacked FDA marketing approval, clearance, or authorization, and the firm failed to notify the agency of intent to introduce these devices into commercial distribution.

Additionally, serology test kits like the "COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma). FDA EUA." and "FDA EUA CE Approved Coronavirus (COVID-19

Company
Avazo-Healthcare, LLC
Inspection date
November 16, 2020
Product type
Devices
Office
Center for Devices and Radiological Health
People
  • Timothy T. Stenzel (Director)
  • Donald D. Ashley (Director)
  • Serena Viswanathan (Associate Director)
View Company Profile

ID · 87328f2d-381b-4455-9fef-24511815d7aa

Violation Codes10
21 U.S.C. 331(a)21 U.S.C. 321(h)21 U.S.C. 351(f)(1)(B)21 U.S.C. 360e(a)21 U.S.C. 360j(g)21 U.S.C. 352(o)21 U.S.C. 360(k)21 U.S.C. 331(k)21.U.S.C. 355(a)21 U.S.C. 352

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