Public COA audit
Kisspeptin-10
Audited September 5, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 72
- Confidence
- 88%
- Panels
- 2/7
Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (2/7), 3 soft concerns, and notable note: "Sterility/microbial testing present". To improve: include identity, purity, and endotoxin at minimum and prefer labs with a public verification portal.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- KSS2607
- Sample date
- 2026-06-30
- Issue date
- 2026-06-30
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.
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.
2 of 7 present · 2 passed · 0 failed · 0 reported · 5 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 certificate file · core
Compound identity confirmed (e.g. HPLC, mass spec).
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.”
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
Tested · passed
Bioburden / microbial limits testing.
No microbial growth detected; Fungi/Yeast Not Detected
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
Tested · passed
Sterility testing where applicable.
No microbial growth detected
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.
Sterility/microbial testing present
Document shows rapid sterility screening with bacteria (aerobic/anaerobic) and fungi/yeast testing, both passing. This is a specialized sterility-focused report.
Limited scope report
This COA only covers sterility/microbial testing. No identity, purity, heavy metals, endotoxin, or residual solvent panels are present. This appears to be a supplemental sterility report rather than a comprehensive COA. Client 'Peptide Partners' may have separate reports for other testing.
Kovera Labs - limited verifiability
Testing lab 'Kovera Labs' is named with professional formatting and QR code/access code (F8A885) for verification, but no URL or contact information is provided on this page to independently verify the lab's credentials or report authenticity.
Same-day turnaround
Sample received and certified on the same date (06/30/2026). While the document states this is a 'rapid' 2-day screening method, same-day certification is unusually fast even for rapid methods and may indicate expedited processing or pre-arranged testing.
Professional presentation
Document has clean, professional layout with clear sections, consistent branding, QR code, and report number (KVR-2026-F8A885). Includes methodology disclosure and regulatory compliance note.
Batch information present
Lot number KSS2607 clearly stated with sample matrix (lyophilized powder) and client information.
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.