Quality & testing

We manufacture our products in a GMP-certified facility and use third-party testing. The summaries below separate manufacturing-system documentation from the results for a specific Calm sample. Supplier-identifying information is withheld from these public brand summaries.

Manufacturing systems

• NSF/ANSI 455-2:2024 GMP facility certification. The supplied certificate includes powder manufacturing and is printed with an expiry date of November 14, 2026.
• HACCP system certification issued by China Quality Certification Centre (CQC). The supplied scope includes supplement powder mixing and is printed with an expiry date of November 13, 2027.
• Food facility registration documentation is on file. FDA registration is separate from product approval; the registration document was privately issued, not issued by FDA.

Facility certifications apply to manufacturing systems and the listed facility scope. They do not mean that each OMIVELLA product is NSF product-certified or FDA approved.

Calm submitted-sample report

Testing period: August 18–22, 2026. The report lists sensory checks (Pass), total bacterial count (<10 CFU/g; specification ≤10,000 CFU/g) and coliform (Negative). Results apply to the submitted sample only. Heavy metals and active-ingredient potency are not listed in this report.

These graphics are brand-prepared summaries, not replacement certificates or laboratory reports. For a documentation inquiry, contact our team.