CDC Shuts Down PCR Test Diagnostic Reports After it Gets Caught Using a Fake Lab-Concocted Coronavirus Simulation to Conduct All Studies!

The CDC developed a test in February 2020 called the “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel” to identify the coronavirus in humans.

In August 2021, the CDC announced it was shutting down the rapid test along with the periodic public release of its performance analysis.

Why are they doing this all of a sudden? The CDC claims it is a “highly accurate test,” after all.

The official given justification is that there are newer and better tests available now that weren’t when this one was developed last year, but perhaps the real reason for shutting down the test and all public releases regarding its performance is that:

The CDC’s own report admits the test was developed and related studies were conducted without even using a real sample of the coronavirus!

The latest report, released July 21, 2021, from the CDC on the rapid test’s performance can be accessed on the FDA’s official .gov website. (The CDC operates under the FDA). On page 40, the CDC reveals it used spoofed virus isolates mixed with human cells in a lab to develop the test.

Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/µL) spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen.

TRENDING: Oregon Senators Demand Grand Jury Investigation into Corrupt CDC and FDA Handling of Coronavirus

Read the full PDF from the FDA below.

EUA-CDC-Panel-IFU

This July 2021 report was revision number seven to the test and remains the version accessible on the FDA’s website. But elsewhere on the internet remain two other full documents: revisions two and three.

Revision number two, published March 15, 2020, can be found on a Texas biotechnology company named Attogene’s website. Revision number three, published two weeks later, can be found on a Mexican university’s website.

The two documents feature both identical wording confirming that “no quantified virus isolates of the 2019-nCoV are currently available” at the time of conducting tests and studies. The only change in wording from this section between revisions two and three and revision seven is the fact that when revision seven was published (in July 2021) there were virus isolates available but they were simply not used.

There has been copious evidence for many months now that these tests are not effective as the CDC claims.

ABC7 Sarasota reported last summer that Florida residents who did not even take the test recieved a message days later notifying them they tested positive for the coronavirus.

Perhaps we will get answers once the investigation two Oregon senators are launching into the FDA and the CDC for covering up coronavirus deaths gets underway.

And this is not unique to America.

A Spanish news outlet ran a recent segment exposing the fraud of rapid coronavirus tests and their consequences when implemented across society.

Everything is a joke. Nothing is real.

This is Biden’s America.

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Resources:

Read the ‘Revision 02’ from Attogene below.

CDC-RT-PCR-eval-nCoV-IFU2-WP-1

Read the ‘Revision 03’ from UNSIS below.

EUA-CDC-nCoV-IFU-1

Read the ‘Revision 07’ from the FDA below.

EUA-CDC-Panel-IFU-3

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