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Guberman to Business Owners, Implant Patients: Your ISO 9001,ISO 13485 AS9100,AI9100 Certificate Is Dead, and Nobody Knows What's Inside You
Rezul News/10746127
Speaking Directly To Business Owners And Implant Patients, 40-Year Quality Expert And Boeing Shareholder: Daryl Guberman Says The September 4, 2018 DOS Contract 19AQMM18R0131 Broke The Accreditation Chain Behind Every ISO Certificate — Leaving Manufacturers Legally Exposed, Patients Unknowingly What's Inside Their Bodies, And Boeing Building Planes Alongside Its Own Regulator.
EVERETT, Wash. - Rezul -- MANUFACTURING ENVIRONMENTS ARE STILL COMPROMISED
My name is Daryl Guberman a Boeing shareholder. I have worked in quality for 40 years, and I live by one rule: in quality you don't lie, because people die. So I'm going to tell you what your registrar never will. I hold the documentation:
The Global Recognition Mandate
In March 2014, the Vice President of ANAB and Chairman of the IAF (incorporated in Delaware) stated that international agreements (MRAs/MLAs) equivalent to ANAB adhere to the global trade mantra: "certified once, accepted everywhere." This foundational mechanism forces signatory countries to automatically trust and legally accept each other's certificates. Because the global system is completely interconnected under this mandate, a single fraudulent or compromised underwriter designation at the top legally breaks the chain, shattering international trust and destroying the validity of cross-border agreements worldwide.
September 4, 2018, the Department of State signed Contract 19AQMM18R0131 naming ANSI-ANAB as "underwriter." As I read ISO/IEC 17011 — Conformity assessment: Requirements for accreditation bodies accrediting conformity assessment bodies
ISO/IEC 17011 defines:
More on Rezul News
ISO/IEC 17011 forbids it.
ANAB violated it.
Once ISO/IEC 17011 is broken, every certificate, every audit, and every conformity decision downstream becomes contaminated. the standard governing accreditation integrity.
Because of this fraud, all certifications issued under ANAB or their MRA/MLA-Multi-Regional-Lateral international equivalents from September 4, 2018 to the present are compromised. Nobody told the employees of ANSI-ANAB about the designation of underwriter on the DOS contract. Nobody told the MRA-MLA international equivalent accreditation bodies, Nobody told the registrars. Nobody told the auditors who work for the registrars, which means any corrective action given to a companies quality system is invalid, Nobody told the OEM's (original equipment manufacturers) or the suppliers, Nobody told the investors, insurers, logistics in medical, automotive, aerospace, etc.
INVESTORS https://youtu.be/PFcghXEoZ9g
As a result, companies worldwide have unknowingly produced goods in environments that cannot be validated and still cannot be validated no accreditation body can legally be an underwriter. That one word, in my finding, severed the chain of authority behind every certificate issued since. So to every business owner who treats that certificate as a nuisance — a plaque on the wall — HEAR ME!- you unknowingly, signed the death warrant for every part you've produced since September 4, 2018. Hop up and down all you want about how good your parts are. Legally, your parts stand on that certificate, and that certificate is dead. The worst part is your registrar never knew the accreditation body perpetrated a fraud and no one knew not even you.
More on Rezul News
Now let me talk to you — the one with the implant. The hip, the knee, the stent, the dental post put into your body any time from September 4, 2018 to today. Based on what I've documented, I need you to understand something: we really don't know what's inside your body. The fraud wasn't committed by the implant makers — it was committed ON them. They never knew. Their auditors never knew. So the chain of custody for every constituent, every material, every process inside that device is broken, and nobody — not the manufacturer, not the insurer, not the materials supplier — can tell you with legal certainty what you're carrying around inside you.
Federal Contract Records Reveal ANAB's 14 Year Accreditation Identity Breakdown: DOS 19AQMM18R0131 (2018) and DOJ 15F06725C0000139 (2025) https://www.prlog.org/13142907-federal-contract-records-reveal-anabs-14-year-accreditation-identity-breakdown-dos-19aqmm18r0131-2018-and-doj-15f06725c0000139-2025.html
And don't look to the FAA to save you. I have documented that the FAA sits on the ANSI-ANAB boards right alongside Boeing — the regulator at the same table as the regulated, building planes in cahoots while suspected unapproved parts flow through the system. That's why I filed 13 Inspector General complaints. So understand the full picture: your parts, your implants, your airplanes — all of it produced in the same compromised environment my documentation exposes, every single day since September 4, 2018. I have the documentation, and I'm not going away The business owner and implant individuals you have legal rights since the meter is still running. Contact Daryl Guberman, 203 556 1493
My name is Daryl Guberman a Boeing shareholder. I have worked in quality for 40 years, and I live by one rule: in quality you don't lie, because people die. So I'm going to tell you what your registrar never will. I hold the documentation:
The Global Recognition Mandate
In March 2014, the Vice President of ANAB and Chairman of the IAF (incorporated in Delaware) stated that international agreements (MRAs/MLAs) equivalent to ANAB adhere to the global trade mantra: "certified once, accepted everywhere." This foundational mechanism forces signatory countries to automatically trust and legally accept each other's certificates. Because the global system is completely interconnected under this mandate, a single fraudulent or compromised underwriter designation at the top legally breaks the chain, shattering international trust and destroying the validity of cross-border agreements worldwide.
September 4, 2018, the Department of State signed Contract 19AQMM18R0131 naming ANSI-ANAB as "underwriter." As I read ISO/IEC 17011 — Conformity assessment: Requirements for accreditation bodies accrediting conformity assessment bodies
ISO/IEC 17011 defines:
- Impartiality
- Structural independence
- Conflict‑of‑interest prohibitions
- Mandatory separation between accreditation bodies and the entities they oversee
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ISO/IEC 17011 forbids it.
ANAB violated it.
Once ISO/IEC 17011 is broken, every certificate, every audit, and every conformity decision downstream becomes contaminated. the standard governing accreditation integrity.
Because of this fraud, all certifications issued under ANAB or their MRA/MLA-Multi-Regional-Lateral international equivalents from September 4, 2018 to the present are compromised. Nobody told the employees of ANSI-ANAB about the designation of underwriter on the DOS contract. Nobody told the MRA-MLA international equivalent accreditation bodies, Nobody told the registrars. Nobody told the auditors who work for the registrars, which means any corrective action given to a companies quality system is invalid, Nobody told the OEM's (original equipment manufacturers) or the suppliers, Nobody told the investors, insurers, logistics in medical, automotive, aerospace, etc.
INVESTORS https://youtu.be/PFcghXEoZ9g
As a result, companies worldwide have unknowingly produced goods in environments that cannot be validated and still cannot be validated no accreditation body can legally be an underwriter. That one word, in my finding, severed the chain of authority behind every certificate issued since. So to every business owner who treats that certificate as a nuisance — a plaque on the wall — HEAR ME!- you unknowingly, signed the death warrant for every part you've produced since September 4, 2018. Hop up and down all you want about how good your parts are. Legally, your parts stand on that certificate, and that certificate is dead. The worst part is your registrar never knew the accreditation body perpetrated a fraud and no one knew not even you.
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Now let me talk to you — the one with the implant. The hip, the knee, the stent, the dental post put into your body any time from September 4, 2018 to today. Based on what I've documented, I need you to understand something: we really don't know what's inside your body. The fraud wasn't committed by the implant makers — it was committed ON them. They never knew. Their auditors never knew. So the chain of custody for every constituent, every material, every process inside that device is broken, and nobody — not the manufacturer, not the insurer, not the materials supplier — can tell you with legal certainty what you're carrying around inside you.
Federal Contract Records Reveal ANAB's 14 Year Accreditation Identity Breakdown: DOS 19AQMM18R0131 (2018) and DOJ 15F06725C0000139 (2025) https://www.prlog.org/13142907-federal-contract-records-reveal-anabs-14-year-accreditation-identity-breakdown-dos-19aqmm18r0131-2018-and-doj-15f06725c0000139-2025.html
And don't look to the FAA to save you. I have documented that the FAA sits on the ANSI-ANAB boards right alongside Boeing — the regulator at the same table as the regulated, building planes in cahoots while suspected unapproved parts flow through the system. That's why I filed 13 Inspector General complaints. So understand the full picture: your parts, your implants, your airplanes — all of it produced in the same compromised environment my documentation exposes, every single day since September 4, 2018. I have the documentation, and I'm not going away The business owner and implant individuals you have legal rights since the meter is still running. Contact Daryl Guberman, 203 556 1493
Source: GUBERMAN-PMC,LLC
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