SodaPeak Testing Standards: Lab Assays & cGMP Compliance
How Peak Vitality Distribution, LLC maintains clinical-grade quality assurance, raw material quarantine, and analytical chromatography verification.
Manufacturing Facility Certification
Every container of SodaPeak is formulated, encapsulated, and packaged within a domestic facility registered with the US Food and Drug Administration (FDA) and audited under 21 CFR Part 111 (Current Good Manufacturing Practice for Dietary Supplements).
Analytical Testing Protocols
1. High-Performance Liquid Chromatography (HPLC-UV)
Used to quantitatively verify botanical active yield and guarantee that each batch delivers 99.4% active botanical vitality yield verification by HPLC-UV. This ensures batch-to-batch consistency and potency.
2. Inductively Coupled Plasma Mass Spectrometry (ICP-MS)
Screens for heavy metals (Lead, Cadmium, Arsenic, and Mercury) to ensure compliance with strict USP <2232> limits (Below 0.05 ppm lead/cadmium/arsenic (Passes USP <2232>)).
3. Total Microbial & Pathogen Screening
Tests for aerobic bacteria, yeast, mold, Salmonella, and E. coli in accordance with USP <2021> and <2022> to guarantee clean microbiological safety.
Third-Party Accreditation
All final release testing is performed by Cascadia BioAnalytical Laboratories, ISO/IEC 17025 accredited, an independent analytical testing organization holding ISO/IEC 17025 accreditation for chemical and biological testing. Master release certificate: CBA-26-9221.