WASHINGTON - TelAve -- .EXPOSED THE LARGEST INDUSTRY & FIDUCIARY FRAUD 2018 TO PRESENT

Guberman to Business Owners, Implant Patients: Your ISO 9001, ISO 13485 AS9100, AI9100 Certificate Is Dead, and Nobody Knows What's Inside You https://www.prlog.org/13171971-guberman-to-business-owners-implant-patients-your-iso-9001iso-13485-as9100ai9100-certificate-is-dead-and-nobody-knows-whats-inside-you.html

Now let me tell you why every word of it is true

Let  me take you back to March 2014. The Vice President of ANAB — who was also the Chairman of the IAF — put it in writing. He explained the whole MRA/MLA game: that's the Mutual Recognition Arrangement and the Multilateral Recognition Arrangement, the system that makes international accreditation bodies equivalent to ANAB. And he gave us the keyword — "certified once, accepted everywhere." Sounds nice, right? Well, that keyword is what corrupted the entire system. Because here's what it really means: the day ANAB committed its fraud, every equivalent body's certificates turned to junk. UKAS over in England — junk. DAkkS in Germany — junk. CNAS in China — junk.and others. All of them. And let me tell you, there is no magic wand on this earth that can go back and fix that.

Now here's the fraud itself, and I'll keep it plain. September 4, 2018. The Department of State signs contract 19AQMM18R0131, and it names ANSI-ANAB as "underwriter." Problem is, ISO/IEC 17011 — the standard that governs accreditation bodies — says no accreditation body can ever be an underwriter. Ever. And only a chosen few at the very top of ANSI-ANAB ever issued that word. Nobody told the ANSI-ANAB employees. Nobody told the MRA/MLA international equivalent accreditation bodies overseas. Nobody told the registrars. Nobody told the auditors — which means every corrective action handed out in a certification audit, surveillance audit, and recertification audit since September 4, 2018? Invalid. All of it. Nobody told the OEMs or their suppliers. Nobody told the investors, the insurers, or the logistics people across medical, aerospace, automotive, electronics, and pharmaceutical. Eight years of parts and medications, all over the world, sitting on compromised certificates. And oh, they tried the name-change trick — IAF Inc. out of Delaware and ILAC out of Australia ( were an association of MRA-MLA accreditation bodies) merged in January 2026 into GLOBAC, Global Accreditation Cooperation and AS9100 magically turned into AI9100. Listen to me: a name change doesn't fix fraud.

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Now, business owner — yeah, I'm talking to you, the one who treats that quality certificate like a nuisance, a plaque on the wall. You need to hear this: without even knowing it, you signed the death warrant for every part you've produced since September 4, 2018. Go ahead, hop up and down about how good your parts are — I've heard it all. Legally, your parts stand on that certificate, and that certificate is dead, invalid a FRAUD. And here's the kicker — your registrar never knew either about the DOS contract underwriter fraud. The accreditation body pulled the fraud and nobody knew, not even you. But you know now. So if you keep producing? That's negligence, friend.

And now let me talk to you — the one with the implant. The hip, the knee, the stent, the dental post they put in your body sometime after September 4, 2018. I've documented a disaster for you and your family, and I need you to really hear me: WE don't know what's inside your body. Nobody does. The fraud wasn't committed by the implant maker or the materials manufacturer or anybody in that chain — it was committed ON them. They never knew. Their auditors never knew. So the chain of custody — every constituent material, every process inside that device — is broken. Not the manufacturer, not the insurer, not the material supplier, not the investor — nobody can tell you with legal certainty what you're carrying around inside you. That ought to shake you to the core!

Now, I keep mentioning the federal procurement record, so let me explain what that means in plain language. GOVLY — most folks have never heard of it — is an AI-powered intelligence platform for federal procurement. It watches government contracts, tracks awards, and puts out what they call "signals," which is basically early intelligence on what's happening in federal contracting. They took my information and published it as Signal #163758 — meaning this fraud case is now sitting in a federal procurement intelligence system where contractors, agencies, and everybody watching government spending can see it. That's the record. Go look for yourself: https://app.govly.com/public/signals/163758

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And then there's the sam.gov world. sam.gov is the federal government's official contracting system — that's where Washington posts its opportunities and awards, the official record of who's doing business with the government. A sam.gov-related news page picked up my case and ran it under the headline "Federal Agencies Face Oversight Failures in Accreditation Processes" — that's the federal contracting press saying, in plain English, that the agencies failed at oversight. Read it yourself: https://samsearch.co/government-contracting-news/federal-agencies-face-oversight-failures-in-accreditation-processes-106805

So let me bring this home. The meter is still running. The fraud is still going, right now, today. Federal agencies and big corporations sit on ANSI-ANAB's board, paying money into a company that pulled a fraud on a federal contract back in 2018 — and they're still paying. And if you think the courts hand out pocket change, think again. The American Medical Association says juries are increasingly handing down "nuclear verdicts" — that's over $10 million — in medical malpractice cases, with the average of the top 50 verdicts climbing from $32 million in 2022 to $56 million in 2024. The compensatory award? That's just the beginning. So get an attorney. I'll be your expert witness. Take it to a jury trial.

CONTACT:  DARYL GUBERMAN - 203 556 1493