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-only report". To improve: include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- TES202607
- Issue date
- 2026-06-22
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 · 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 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 · passed · core
LAL or chromogenic endotoxin assay.
<10.0 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-only report
This COA is scoped to endotoxin testing only (USP <85>). No purity, identity, heavy metals, microbial, sterility, or residual solvent panels are present on this document. This appears to be a split report for endotoxin testing specifically, which is common practice. The vendor may have separate reports for purity/identity testing.
Legitimate testing laboratory
TrustPointe Analytics LLC is a known third-party testing laboratory in Dorr, MI with verifiable contact information and online presence. The document includes a verification URL and key for independent confirmation.
Client sample ID present
Client SID TES202607 and internal lab ID SPL-4250 are both documented.
Endotoxin test passed
Bacterial endotoxin result of <10.0 EU/mL with acceptable spike recovery (85%) and CV values (0.0% sample, 2.2% spike) indicates passing endotoxin testing per USP <85> methodology.
Professional presentation
Document includes QR code for verification, dual signatures (President and Managing Director), complete lab contact information, and proper USP method citations.
No purity data on this report
This document does not contain HPLC purity, identity confirmation, or other compositional analysis. For complete quality assurance, a separate purity/identity COA should exist for this lot.
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.