Public COA audit

NAD+

Audited September 5, 2026

Incomplete documentation

Missing panels or key metadata — not enough evidence to treat this as a full certificate.

Legitimacy
45
Confidence
75%
Panels
1/7

Scored poorly because the file is incomplete or not a full COA, limited panel coverage (1/7), 1 critical finding, and notable note: "No purity data provided". To improve: upload the full certificate (or the matching sibling purity/endotoxin report) and include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
FNAD1000F041825
Identity method
qualitative and quantitative analysis
Sample date
2025-04-29
Issue date
2025-05-02

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.

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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.

1 of 7 present · 0 passed · 0 failed · 1 reported · 6 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 · result on file · core

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

    qualitative analysis performed

  • Purity

    Not on this certificate file · core

    Reported purity percentage for the analyte.

    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.”

  • Heavy metals

    Not on this certificate file

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

  • 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

    Not on this certificate file · core

    LAL or chromogenic endotoxin assay.

    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.”

  • 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.

  • No purity data provided

    Report shows only mass measurements (1109.30 mg, 1109.71 mg, 1445.69 mg) without any purity percentage, HPLC chromatogram, or assay result. Cannot determine product quality.

  • Identity testing method unclear

    States 'qualitative and quantitative analysis of non-AAS sample' but provides no spectral data, mass spec, NMR, or other identity confirmation. Only mass values are shown.

  • Minimal testing scope

    This report only covers basic identity/quantitation. No purity, heavy metals, microbial, endotoxin, sterility, or solvent testing is included. This may be a partial report or basic screening only.

  • Incomplete results presentation

    Results section shows three mass values with no context, units explanation, or interpretation. Empty rows in results table suggest incomplete data entry or missing information.

  • Verification system present

    Document includes verification URL (www.janoshik.com/verify/) with unique key RC91EP2CY4QM and QR code for authentication.

  • Dates are reasonable

    Testing ordered 24 APR 2025, sample received 29 APR 2025, analysis conducted 02 MAY 2025. Timeline is logical and all dates are in the past relative to 2026-09-05.

  • Batch number present

    Batch FNAD1000F041825 is clearly documented.

Timing & next steps

Practical follow-ups based on document age and gaps.

  • coa age

    This COA was issued over a year ago (491 days) — consider whether a retest is warranted for this batch.

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.