Pfizer BioNTech and Moderna produce "vaccines" that fail production quality standards - and people are dying because of it.

Must read!

https://open.substack.com/pub/hedleyrees/p/the-inside-story-on-dna-vaccine-supply-fdb

Hadley Rees of Inside Pharma has exposed the appalling quality standards in the manufacturing of “vaccines” of both Moderna and Pfizer-BioNTech.

BioNTech is now controlled by the Chinese Communist Party. Along with Moderna, it is a start-up company - financed by “vulture funds” at the EU) State and private individual levels.

Not only are the “vaccines” toxic when they are produced correctly, they are even more toxic when they are produced incorrectly.

This can be correlated with data from howbadismybatch.com

US Federal regulators have the ability to prosecute but are criminally negligent in enforcing laws they are tasked with enforcing.

A reminder from here:

Recall of Moderna C19 Injections? - by Peter Halligan (substack.com)

https://peterhalligan.substack.com/p/recall-of-moderna-c19-injections

..to the Moderna quality breaches. Here is a link to the FDA Form 483 report resulting from an onsite inspection conducted during August 2022

download (fda.gov)  https://www.fda.gov/media/161643/download

Mr Hedley does a great job critiquing the implications of the reports findings. Here are Observations 1, 3 and 4 from the twelve raised in the FDA Form 483.

OBSERVATION 1

Your firm failed to thoroughly investigate any unexplained discrepancy or failure of a batch or any of its components to meet any of its specifications, whether or not the batch has already been distributed.

OBSERVATION 3

Control procedures are not established which monitor the output and validate the performance of those manufacturing processes that may be responsible for causing variability in characteristics of the in-process material and the drug product.

OBSERVATION 4

Acceptance criteria for the sampling and testing conducted by the quality control unit is not adequate to ensure that batches of the drug product meet appropriate statistical quality control criteria as a condition for their approval and release.

Suffice to say, it begs the question:

“Why are there product recalls with the potential for harm in the baby formula, auto and aviation industries, whereas there is no recall for C19 injections causing actual harms to millions of Americans which contain toxic substances at unknown levels and instructions for the body to create unknown numbers of toxins?”

In the US, this quality control is captured by laws like those cited below – breaches of these are violations of Federal Law – where is the FBI?:

21 U.S. Code § 351 - Adulterated drugs and devices | U.S. Code | US Law | LII / Legal Information Institute (cornell.edu)

https://www.law.cornell.edu/uscode/text/21/351

21 U.S. Code § 360d - Performance standards | U.S. Code | US Law | LII / Legal Information Institute (cornell.edu)

Definition: device from 21 USC § 321(h)(1) | LII / Legal Information Institute (cornell.edu)

Here are the section headings from Code 351:

“A drug or device shall be deemed to be adulterated—

(a)Poisonous, insanitary, etc., ingredients; adequate controls in manufacture

(b)Strength, quality, or purity differing from official compendium

(c)Misrepresentation of strength, etc., where drug is unrecognized in compendium

(d)Mixture with or substitution of another substance

(e)Devices not in conformity with performance standards

(f)Certain class III devices

(g)Banned devices

(h)Manufacture, packing, storage, or installation of device not in conformity with applicable requirements or conditions

(i)Failure to comply with requirements under which device was exempted for investigational use

(j)Delayed, denied, or limited inspection; refusal to permit entry or inspection

There is much more detail describing each of these section headers - quality must be monitored by the regulator. Evidence of such monitoring and quality assurance? Well, the www.howbadismybatch.com provides a wealth of evidence that this is not the case.

An extract from the “States” tab of How Bad is my Batch ?:

“Some states, in particular Kentucky, Montana, Alaska, Tennessee, North Dakota and South Dakota are experiencing 4 x, 5 x, 6 x or even 11 x the number of deaths per 100,000 vaccinated compared to other states. Such a situation should be raising a safety signal, and requires investigation. The higher death rate in these states following vaccination suggests that they may be receiving more toxic batches, or being administered to more vulnerable people.”

Here is a reminder of another article from July 2022.

FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal • Children's Health Defense (childrenshealthdefense.org)

https://childrenshealthdefense.org/defender/fda-moderna-bypass-covid-vaccine-safety-standards-documents/