Public COA audit
AOD-9604
Audited July 29, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 92
- Confidence
- 93%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- AO202605
- Issue date
- 2026-04-20
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 · 1 passed · 0 failed · 0 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
Not on this COA · core
Compound identity confirmed (e.g. HPLC, mass spec).
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Purity
Not on this COA · core
Reported purity percentage for the analyte.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Heavy metals
Not on this COA
Lead, arsenic, cadmium, mercury, or similar limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Microbial
Not on this COA
Bioburden / microbial limits testing.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Endotoxin
Tested · passed · core
LAL or chromogenic endotoxin assay.
< 0.08 EU/mL
Sterility
Not on this COA
Sterility testing where applicable.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Residual solvent / water
Not on this COA
Residual solvents or water content limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
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
Not on this certificate. Lowers thoroughness; you decide if that panel matters for your use case. PeptIQ’s score still factors coverage.
Findings
Evidence-linked observations from this audit.
Endotoxin testing complete
Comprehensive bacterial endotoxin analysis performed using USP <85> kinetic chromogenic LAL assay with proper controls and validation metrics (CV, spike recovery). Result < 0.08 EU/mL passes acceptance limit of ≤ 0.5 EU/mL.
Limited scope COA
This is a single-panel endotoxin report only. No identity, purity, heavy metals, microbial, sterility, or residual solvent testing included. This is common for supplemental testing but not a complete characterization COA.
Professional lab presentation
Kovera Labs report shows professional formatting, proper methodology documentation, QC controls (positive/negative), validation metrics (CV%, spike recovery), and verification URL with access code.
Batch information present
Lot/Batch AO202605 clearly documented with product name AOD-9604, strength 10 mg, lyophilized condition.
Analysis date documented
Analysis date 04/20/2026 is clearly stated and falls within reasonable timeframe (before today's date of 2026-07-28).
Proper authorization
Report signed by Lemar Arghandiwal, Lab Director, with sample ID KVR-2026-803483 and access code for verification.
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.