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Documentation your auditor can follow line by line.

Quality at JayB Food Labs is a records-first system. Every lot we produce is reconstructable from receipt of raw material to the case that leaves our dock.

FDARegistered food facility, subject to inspection.
CDPHCalifornia Food & Drug Branch registered.
111/117cGMP per 21 CFR Parts 111 and 117.
Lot-levelTraceability with recall readiness.
Gowned operator reviewing a checklist beside production equipment
Registrations & framework

Registered, inspected, and run to written procedure.

  • FDA Food Facility Registration — registered and subject to inspection by the U.S. Food & Drug Administration.
  • California Department of Public Health — registered with the CDPH Food and Drug Branch.
  • cGMP — 21 CFR Parts 111 & 117 — manufacturing, packaging, labeling, and holding operations under current Good Manufacturing Practice.
  • Standard operating procedures — every recurring operation, from gowning to line clearance, runs to a controlled SOP.
QC inspector documenting observations on the production floor
Batch documentation

If it isn't written down, it didn't happen.

Every product has a master manufacturing record; every lot has a batch production record. In-process checks — fill weights, seal torque, metal detection, label verification — are performed at defined intervals and signed into the record as they happen.

  • Master manufacturing records defining formula, process, and specs.
  • Batch production records with in-process checks and yield reconciliation.
  • Certificate of analysis support for every released lot.
  • Review before release — no lot ships until its record is reconciled.
Material & facility controls

Control at every point where risk enters.

Incoming materials

  • Supplier qualification program
  • Receipt verification & quarantine
  • Release against specification
  • Allergen identification & control

Facility & environment

  • Environmental monitoring
  • Pest control program
  • Validated cleaning procedures
  • Gowning & hygiene SOPs

Traceability & recall

  • Lot-level traceability end to end
  • Mock-recall capable
  • Distribution records per shipment
  • Retained samples per lot
For your auditors

Bring your audit. We'll bring the records.

Brand owners are welcome to qualify us the way they'd qualify any supplier — questionnaires, document requests, and on-site audits. A facility that runs on records has nothing to assemble the night before.

Schedule a qualification call

Quality questions before you commit?

Ask us anything — registrations, procedures, batch documentation. We answer plainly, in writing.

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