Quality
Quality Records Your QA Team Can Review.
Batch records, release testing, COAs, and documentation packages prepared for customer review.
Raw Material
Supplier documents are reviewed before the lot moves into identity and purity checks.
Production
Batch parameters are recorded during reaction, drying, milling, and packing.
In-Process QC
Mid-batch checks track appearance, moisture, solubility, and process consistency.
Release Testing
Finished lots go through assay, free magnesium, moisture, and document review before release.
Warehouse Delivery
Released inventory is matched to COA, lot code, and shipping documentation before dispatch.
Batch traceability
From supplier lot to released COA
Every shipment traces back through four linked records, so your QA team can follow one lot code from raw material to the COA in the drum.
- Step 1Supplier Lot
- Step 2Production Batch
- Step 3QC Record
- Step 4Released COA
- Purity
- 99.8%
- Against the product specification
- Release pass rate
- 99.8%
- Share of lots passing release testing
- In-stock lead time
- About 3 days
- In-stock orders ship from Ontario, California
- Production lead time
- 1–2 weeks
- Production orders for lots not held in stock
- Batch consistency
- Per lot
- COA and records tied to each lot code
Certification wall
GMP
NSF GMP for Sport
FDA Facility
ISO
FSSC
NON GMO
HALAL
KOSHER
GRAS
BRCGSAudit readiness panel
Organized supplier qualification, batch records, specification control, COA review, and customer documentation packages.