Zuluvape Has Moved to the Review Phase of the PMTA Process
Zuluvape is pleased to announce that On November 6, 2020 we received our Premarket Tobacco Product Application (PMTA) Filing Letter from the U.S. Food and Drug Administration. This letter advised us that the FDA has reviewed our PMTA and determined our application meets the filing requirements for new tobacco products seeking a marketing order and contains all items under section 910 of the FD&C Act. This is great news and Zuluvape is moving on to the next phase of the PMTA process. Once again Zuluvape is committed to our loyal adult customers and we will be here to provide the highest quality e-liquids available that is 100% FDA compliant.
