CrazyChef
Custom Hand Crafted Coils - PureCoils.com
VU Vendor
VU Donator
Platinum Contributor
Member For 4 Years
ECF Refugee
As much as I am FOR regulation in the vaping industry, the FDA has obviously gome way overboard in their decisions regarding the regulations concerning the the whole of our industry, and their definitions of what constitutes a regulatable ENDS component.
As I mentioned above, I believe there should be reasonable regulations - no sales to minors being my main concern, as well as end user caution statements on the packaging of products that can be dangerous if used improperly (hybrid series mech mods, for example). But... Have they lost their freaking minds?!?!?
At any rate... Most of you already know that I own a custom coil business. According to the FDA, coils (which are, in their simplest form, just springs) are considered part of the ENDS components and are subject to regulation.
This is absurd.
So...
This thread is a place for all who are unjustifiably being regulated by what the FDA considers to be an ENDS component, and what we can do about it.
What are your thoughts, and what have you learned about loopholes that will positively affect our businesses?
As I mentioned above, I believe there should be reasonable regulations - no sales to minors being my main concern, as well as end user caution statements on the packaging of products that can be dangerous if used improperly (hybrid series mech mods, for example). But... Have they lost their freaking minds?!?!?
At any rate... Most of you already know that I own a custom coil business. According to the FDA, coils (which are, in their simplest form, just springs) are considered part of the ENDS components and are subject to regulation.
This is absurd.
So...
This thread is a place for all who are unjustifiably being regulated by what the FDA considers to be an ENDS component, and what we can do about it.
What are your thoughts, and what have you learned about loopholes that will positively affect our businesses?