Article by Scott Armstrong

Clip from The Daily Wrap-Up by Ryan Cristián: FDA Accidentally Exposes EUA Deception, Ukraine The Runaway Train & Massive Vaccine Risk Cover Up (12/14/2022)

The US Food and Drug Administration (FDA) has historically been looked at to provide rigorous health and safety standards that products must adhere to in order to be considered appropriate for public consumption. Prior to Covid, not many people gave much thought as to whether or not the FDA was operating with the public's best interest in mind. Now that the FDA has been under an incredible amount of public scrutiny, it has become apparent that they have acted with a complete lack of integrity and clearly have motives beyond protecting the public.

In December of 2020, the Covid-19 "vaccine" was released to the public under Emergency Use Authorization (EUA). An EUA is different from an FDA Approval, in that it has not met the rigorous standards needed for "Approval" status. According to the FDA's website:

Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), when the Secretary of HHS declares that an emergency use authorization is appropriate, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency