Why are they lying about their origins? Because, Watt says, "They have maintained a bunch of empty office buildings that serve only as mailing addresses There are no technicians in the buildings, there's no equipment and no sample testing occurs."
"In 1973, FDA published a consolidated set of biological product manufacturing non-regulations in the Federal Register," Watt explained.
My hypothesis is that they have maintained a bunch of empty office buildings that serve only as mailing addresses, without having any actual technical staff, laboratory equipment, or application and sample processing procedures.
The factory employees, who are also just a handful of paper pushers with no scientific knowledge or responsibility, in a building whose equipment just makes immunotoxic junk and puts it in vials and slaps labels on it, filled out the application forms and mailed them to the FDA addresses.
There are no technicians in the buildings, there's no equipment and no sample testing occurs.
It's all a front: statutes, regulations, procedures, application forms, buildings, addresses, offices, labs, approved applications and licenses sent by the FDA back to the factories, everything.
Everyone else just assumes that a different, specialised department with specialised staff, equipment and procedures is handling it somewhere in the factory, and somewhere within the FDA. You can read Watt's full article HERE which is the ninth in a series of articles on "FDA non-regulation of non-medicines, including vaccines, more accurately understood as intentionally immunotoxic poisons."
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