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"We now look forward to re-engaging with the FDA on a science- and evidence-based process to pursue a marketing authorization for Juul products." To sell tobacco products in the United States, companies are required to submit a Premarket Tobacco Product Application that must provide scientific data demonstrating its product is "appropriate for the protection of public health." Nearly two weeks ago, the FDA issued a marketing denial order for Juul's e-cigarette device and four types of Juulpods, stating the company's applications "lacked sufficient evidence regarding the toxicological profile of its products to demonstrate that marketing its products" would benefit the health of the public
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Association between e-cigarette use and asthma: a systematic review and meta-analysis
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