Artisan Vapor & CBD: Premarket Tobacco Application Accepted by the Food and Drug Administration

The Premarket Tobacco Applications within the vape industry have been accepted by the Food and Drug Administration and are now undergoing review!

Online PR News – 29-April-2021 – Dallas, Texas – In September of 2020, the Food and Drug Administration (FDA) received hundreds of Premarket Tobacco Applications (PMTA) from retailers across the United States of America. As one of the largest retailers of vape and CBD products in the country, we at Artisan Vapor & CBD submitted our application for review alongside our peers.

The application provided by us included detailed scientific research demonstrating that our products are appropriate for adult use. We at Artisan Vapor & CBD have always been committed on providing only the highest quality products to users looking for nicotine alternatives.

In April of 2021, we received the news that our application has been accepted for review by the FDA. This means Artisan Vapor & CBD has passed the first stage of the process and is one step closer to the final pronouncement. This acceptance marks an extremely important step in the process.

Following this, the application will move forward towards an in-depth scientific review of the products to determine their eligibility in terms of being appropriate for the protection of public health.
We at Artisan Vapor & CBD strictly follow all guidelines that have been set out by the FDA for the products manufactured by us and continue to maintain the set standard.

The final acceptance by the FDA, which is the next step of the process, will mark Artisan Vapor & CBD as one of the most trusted names in the industry. We will then be able to move forward with providing our customers with alternatives to smoking, including helping them make different lifestyle choices.

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