Potential FDA Regulatory Loophole for Vapor Manufactures

Categories: fda, News, Top Vapor News, VaporBy Published On: September 8th, 202185 words

The vapor industry, regulated as tobacco products by the U.S. Food and Drug Administration (FDA), is facing increasing challenges in getting its products approved for marketing and distribution in the U.S. As required by the FDA, deemed tobacco products–including vapor and e-cigarettes–were required to submit premarket tobacco product applications (PMTA) to the FDA by Sept. 9, 2020.

In a matter of days, the FDA is supposed to approve or deny the thousands of applications it has received.

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