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WARNING LETTER
•Camelot E-Liquid•April 2, 2019

Camelot E-Liquid – FDA Warning Letter, Apr 2, 2019

Record Details

On March 6, 2019, the FDA issued a Warning Letter to Camelot E-Liquid, specifically to James Shearon, following a review of their website, http://cameloteliquid.com. The FDA determined that Camelot King Arthur e-liquid, manufactured and sold by Camelot E-Liquid, is a tobacco product under section 201(rr) of the FD&C Act.

The primary violation identified was the sale of Camelot King Arthur e-liquid to a person younger than 18 years of age, which constitutes misbranding under section 903(a)(7)(B) of the FD&C Act (21 U.S.C. § 387c(a)(7)(B)). This violates 21 C.F.R. § 1140.14(b), which prohibits retailers from selling covered tobacco products, including e-liquids, to minors.

Camelot E-Liquid is required to immediately correct this violation and any similar issues, ensuring all tobacco products and related advertising comply with the FD&C Act and FDA regulations. Failure to comply may result in further FDA actions, including civil money penalties, no-tobacco-sale orders, criminal prosecution, seizure, and/or injunction. A written response detailing corrective actions, including dates of discontinuation of violative sales and a plan for maintaining compliance, must be submitted within 15

Company
Camelot E-Liquid
Inspection date
April 2, 2019
Product type
Tobacco
Office
Center for Tobacco Products
People
  • Ann Simoneau (Director)
  • James Shearon
View Company Profile

ID · a0311bae-6d80-4ca8-a813-553f6b0987c0

Violation Codes6
21 U.S.C. 321(rr)21 U.S.C. 387a(b)21 U.S.C. 387c(a)(7)(B)21 CFR 1140.14(b)21 CFR 1140.321 CFR 1100.2

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