Temperature-conscious packaging · Clean formulations, lab-tested in every batch
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Quality testing at Leandoor

Quality

What’s on the label is what’s in the bottle.

Made in an FDA-registered facility under current Good Manufacturing Practices. Every batch tested for identity, potency, and purity — including heavy-metal screening. Every claim reviewed against substantiation before it ships.

Four pillars. One standard.

  • Lab-tested

    Every batch is tested by analytical labs for identity, potency, and purity — including ICP-MS heavy-metal screening, microbiological testing, and physicochemical testing. Batch traceability is documented end-to-end.

    Source. Manufacturer batch-record + ICP-MS report on file for each production lot.

  • Quality-certified manufacturing

    Manufactured at an FDA-registered facility operating to current Good Manufacturing Practices (cGMP, 21 CFR Part 111). The facility is NSF-GMP registered and ISO 9001:2015 and ISO/IEC 17025:2017 accredited.

    Source. Facility registration + cGMP audit records held by the manufacturing partner.

  • Clean formulations

    Every Leandoor product is Non-GMO and Gluten-Free. We disclose the active ingredients on every Supplement Facts panel, in plain English, with the form and dose.

    Source. Per-SKU ingredient declarations + supplier specifications on file.

  • Plain-English science

    Every PDP shows the full Supplement Facts panel, the active ingredient form and dose, and uses structure/function language only. No outcome promises, no disease claims, no fear-based marketing.

    Source. Internal claims-review policy + the FDA dietary supplement disclaimer site-wide.

The no-list

What we don’t put in our products.

Every Leandoor formulation is built around a small allow-list of ingredients we can substantiate. Here’s what we leave out by design.

  • Artificial colors
  • Artificial sweeteners
  • Artificial flavors
  • Hydrogenated oils
  • GMO ingredients (Non-GMO claim per SKU)
  • Gluten (Gluten-Free claim per SKU)
  • Disease-treatment claims

Certificates & reports

Documents on file.

Per-batch Certificates of Analysis (COAs) link from this section once individual production runs ship. Until then, contact quality@leandoor.com with any specific request.

  • Facility cGMP audit

    21 CFR Part 111 compliance, current audit cycle.

    Document — coming soon

  • Identity & potency

    HPLC / mass-spec verification per active ingredient.

    Document — coming soon

  • Heavy-metal screening

    ICP-MS report per batch, lead / cadmium / mercury / arsenic.

    Document — coming soon

Questions?

Email quality@leandoor.com for documentation requests, or read the FAQ for everything else.

Disclaimer. These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Built for daily use

Eight products, formulated the same way, tested the same way. Browse the line when you're ready.