Public COA audit

Glutathione

Audited September 5, 2026

Evidence suggests fabrication

Multiple signals on this document conflict with known lab formats or verification patterns.

Legitimacy
15
Confidence
92%
Panels
4/7

Scored poorly because audit signals point to fabrication or reused paperwork, limited panel coverage (4/7), 4 critical findings, and notable note: "Mass Spectral Match Failed". To improve: replace this file with an original lab certificate that verifies on the lab portal and include identity, purity, and endotoxin at minimum.

Document details

Fields extracted from the certificate — not order or payment data.

Batch / lot
whm9fzc
Identity method
HPLC-UV-MS
Sample date
2026-06-04
Issue date
2026-06-15

Original certificate

Embedded copy of the stored COA PDF or image. Download it for your records — PeptIQ’s audit is separate from the lab document itself.

Loading original certificate…

7-panel checklist

Had data + good, had data + bad, reported without pass/fail, or missing. Missing lowers thoroughness — you decide whether that panel matters; PeptIQ’s score still factors coverage.

4 of 7 present · 0 passed · 1 failed · 3 reported · 3 missing

Missing is a thoroughness gap — not automatically bad. PeptIQ’s legitimacy score still weighs panel coverage; you can down-weight panels that don’t matter for your use case.

  • Identity

    Tested · failed · core

    Compound identity confirmed (e.g. HPLC, mass spec).

    Incorrect

  • Purity

    Tested · result on file · core

    Reported purity percentage for the analyte.

    ND

  • Heavy metals

    Tested · result on file

    Lead, arsenic, cadmium, mercury, or similar limits.

  • Microbial

    Not on this certificate file

    Bioburden / microbial limits testing.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Endotoxin

    Tested · result on file · core

    LAL or chromogenic endotoxin assay.

  • Sterility

    Not on this certificate file

    Sterility testing where applicable.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Residual solvent / water

    Not on this certificate file

    Residual solvents or water content limits.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

How to read this

Had data · good

Panel present with a pass (or clear acceptance).

Had data · bad

Panel present with a fail — a concrete quality signal.

Had data · unclear

Value reported without an explicit pass/fail mark.

Missing on this file

Not on this certificate file. Lowers file thoroughness; a sibling endotoxin/purity report for the same lot may still exist. PeptIQ’s score still factors coverage.

Findings

Evidence-linked observations from this audit.

  • Mass Spectral Match Failed

    The COA explicitly states 'Mass Spectral Match: Incorrect' — the compound failed identity verification by mass spectrometry. This is a fundamental failure indicating the sample is not the claimed compound (Glutathione).

  • Purity Not Detected

    Chromatographic purity shows 'ND' (Not Detected) with no percentage value. Combined with identity failure, this suggests the sample does not contain the target compound at detectable levels.

  • Glutathione Quantity Not Detected

    The Glutathione quantification row shows 'ND mg' — no measurable amount of the target compound was found in the sample.

  • Vendor/Lab Name Mismatch

    The document header shows 'Finnrick Analytics' and 'Finnrick.com' but the lab performing analysis is 'Krause Analytical LLC' (Austin, TX). The branding is inconsistent — Finnrick appears to be a reseller/vendor, not the testing lab, yet the document is styled as a Finnrick certificate.

  • Unusual Result Presentation

    A legitimate COA would not typically issue a certificate for a sample that completely failed identity and purity testing. The document format suggests this may be a template or fabricated report rather than a genuine analytical result.

  • Methods Listed But No Results

    Page 4 describes methods for Endotoxins (USP/NF 86) and Metals (USP/NF 233), but page 1 shows no actual test results for these panels. This suggests incomplete testing or a template document.

  • Batch/Lot Number Present

    Batch/Lot number 'whm9fzc' is clearly stated and matches across pages.

  • Dates Within Valid Range

    Sample received 2026-06-04, tested 2026-06-09, report issued 2026-06-15. All dates are sequential and on or before the current date (2026-09-05).

PeptIQ COA reports analyze document content and publicly verifiable lab signals. They are educational and not a guarantee of product quality, legality, or safety. Always consult a qualified professional before making health decisions. We never publish purchase prices, shipping details, or uploader identity.