After years of preparing and finally submitting, on January 20, 2021, 7 Daze® was issued an Acceptance Letter for its Premarket Tobacco Product Application (PMTA) of Reds Apple® products by the U.S. Food and Drug Administration (FDA). This now places 7 Daze® into the substantive review phase.
All manufacturers of electronic nicotine delivery systems (ENDS) were required to submit a PMTA to the FDA by the September 9th, 2020 deadline to continue selling ENDS products in the United States. During the substantive review phase, the FDA evaluates the scientific studies and data presented in the applications submitted to ensure that the products are appropriate for the protection of the public health (APPH). 7 Daze® will continue working with the FDA until all necessary requirements are met, resulting in the company being granted a marketing order.
Here at 7 Daze, we strive to provide responsible alternative products for adult smokers worldwide. We want to thank our valued 7 Daze customers and partners as we will continue to maintain the highest-quality products and services, providing you with the ultimate vaping experience.
If you have any questions or concerns, please feel free to Contact Us.