Public COA audit
Tesamorelin
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
- 1/7
Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (1/7), 2 soft concerns, and notable note: "Endotoxin testing present". To improve: include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- TES202601
- Issue date
- 2026-01-06
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.
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
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
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.
11.0 EU/mL
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.
Endotoxin testing present
USP <85> bacterial endotoxin testing performed with result 11.0 EU/mL, sample CV 2.6%, spike CV 2.1%, spike recovery 85%. This is an endotoxin-only report.
Limited scope report
This COA only covers endotoxin testing. No purity, identity, heavy metals, microbial, sterility, or residual solvent panels are present on this document. This appears to be a split report focusing solely on endotoxin analysis.
Batch/lot identified
Client SID TES202601 clearly stated
Issue date present
Published 2026-01-06 08:35, which is before the current date of 2026-09-05
Lab identification
TrustPointe Analytics LLC with full address (1743 142nd Ave Suite 4, Dorr, MI 49323), phone (616-359-9023), email, and website provided
Verification system
QR code and verification URL (TrustPointeLIMS.com) with key HPVLJXHMSNS4 provided for independent verification
Professional presentation
Document includes signatures from Ashlee Lust (President) and Joshua Lust (Managing Director), professional layout with TrustPointe branding
Pass/fail not explicitly stated
Endotoxin result of 11.0 EU/mL is reported with USP limit reference (5 EU/kg/hr), but no explicit pass/fail determination is stated on the document
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.