Those are now working.
Skimming over the proposed FDA deeming regulations, it was readily apparent to me that the FDA doesn't have a clue with what they are dealing with. How they can propose that all devices manufactured after 2007 require individual applications & approvals and reasonably expect to be able to handle all of the massive data that will come their way within a reasonable time is beyond reason. They are without a doubt ignorant and uneducated about the industry and unaware of the impact that they will have on the industry with their ill-prepared regulations.
Who could be better to educate them than CASAA? To EVERYONE who is reading this post, PLEASE join CASAA if you are not already a member. They will be our advocate and representative in this debacle with the FDA. CASAA's strength is in their membership numbers of vapers whom they represent. It's extremely important that you be a member. They are volunteers who are in the front line of this political battle.
The link to join for free is in the link in my signature below.