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Re: Wazer post# 20363

Thursday, 09/21/2017 11:51:37 AM

Thursday, September 21, 2017 11:51:37 AM

Post# of 20669
Let me address the FDA situation:

Inojex model 30 is a class 11 device, as such it is not required to have Formal FDA APPROVAL to fall under the governance of the FDA. However, there are different categories within the FDA governance, from what this product actually has to FORMAL FDA PRODUCT APPROVAL like so many products actually legally have which inojex 30 does not have. As most probably know, formal FDA product approval can take years, exhaustive clinical trials and unbelievable amounts of money, none of which inojex model 30 went through.
INOL can sell this product under the governance of the FDA by stating that the product has "FDA CLEARANCE OR FDA LISTED" but absolutely cannot falsely or fraudulently market the product as having "FDA APPROVAL".

Berthold and associates were presented in 12/2015 prior to any SPA ARRANGEMENT being executed that the injex 30 product had FDA APPROVAL and 5 million dollars in revenue, neither is true nor can inol legally state that this product ever had or has FDA PRODUCT APPROVAL. Berthold and all shareholders were presented with fraudulent information from the onset.
Let's remember that this current group has accepted investment dollars, issued a private placement memorandum, issued false filings all under the fraudulent FDA CLAIMS.

Can you imagine one of your family members using a product that purportedly has FDA APPROVAL, and that family member has some adverse reaction (unusual or not) and that individual finds out that the product and the company selling the product where and are mis-stating what FDA approvals that product had or did not have?
The legal action that would follow would be mind boggling. I do not know if INOL could remotely afford liability insurance to cover themselves properly, especially since they stiffed ParkerPoe.

Everyone can simply validate this with a call to the FDA.

WHILE YOU ARE VALIDATING THIS INFORMATION SEE IF YOU CAN VALIDATE WHAT WAS STATED IN INOLS DEFINITIVE AGREEMENT OF FEBRUARY 2016 SIGNED BY HUGHES BENOIT AND JOHN ODA,
FDA VERSION NUMBER- M GBA EN FR RO1 1209SFR

I have not been able to locate this above number anywhere.
Potentially just more fraud!