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WARNING LETTER
•The Clean Vape•March 12, 2021

The Clean Vape – FDA Warning Letter, Mar 12, 2021

Record Details

The FDA Center for Tobacco Products issued a Warning Letter to Raffy Tasmajian, operating TheCleanVape.com, after determining that e-liquid products listed on the website are manufactured and offered for sale or distribution in the U.S. These e-liquids, including "Loops," "Dragonberry Kiwi," and "Gramberry," are considered "new tobacco products" under section 201(rr) of the FD&C Act and are subject to FDA regulation. The firm failed to obtain the required premarket marketing authorization order under section 910(c)(1)(A)(i) of the FD&C Act, rendering these products adulterated under section 902(6)(A) and misbranded under section 903(a)(6) because the required notice or information under section 905(j) was not provided. Despite being a registered manufacturer with over 800 listed products, the firm did not comply with these critical regulatory requirements. The FDA requires a written response within 15 working days detailing corrective actions, including discontinuing violative activities and a plan for future compliance. Failure to address these violations may result in civil money penalties, product seizure, injunction, and refusal of admission for imported products.

Company
The Clean Vape
Inspection date
March 12, 2021
Product type
Tobacco
Office
Center for Tobacco Products
People
  • Ann Simoneau (Director)
  • Raffy Tasmajian
View Company Profile

ID · 894fc9c9-b62c-4f9c-aa91-a77570f1abb1

Violation Codes10
21 U.S.C. 321(rr)21 U.S.C. 387a(b)21 U.S.C. 387j(a)21 U.S.C. 387j(c)(1)(A)(i)21 U.S.C. 387e(j)21 U.S.C. 387e(j)(1)(A)(ii)21 U.S.C. 387e(j)(3)21 U.S.C. 30121 CFR 1100.121 CFR 1140

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