Hi everyone! Fell off the wagon for a while, hopped back on (holding on tight), and now I'm learning about all of this FDA stuff. I've been lurking around, reading articles that others have posted, and reading through some big posts about it. I just want to make sure what I'm reading is actually registering appropriately in my head (honestly, I keep reading vague articles, so I'm not sure I'm getting BIG PICTURE here).
So, August 8th, 2016, deeming goes into effect? Do things go flying off the shelves at this time? And companies must submit applications on their products, their safety, why they should stay on the market, etc? And each costs a ridiculous amount of money... those companies and small b&m's that make their own juices... if they can't afford the price tag of the app, do they have to shut down their juice-making operation as of August 8th? And this application thing is a 2 year process, right?
If anyone has a good in depth article that explains the steps behind vapocalypse, that'd be great, too!
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So, August 8th, 2016, deeming goes into effect? Do things go flying off the shelves at this time? And companies must submit applications on their products, their safety, why they should stay on the market, etc? And each costs a ridiculous amount of money... those companies and small b&m's that make their own juices... if they can't afford the price tag of the app, do they have to shut down their juice-making operation as of August 8th? And this application thing is a 2 year process, right?
If anyone has a good in depth article that explains the steps behind vapocalypse, that'd be great, too!
Sent from my SM-G925P using Tapatalk