Frequently asked questions

We support USDA Organic, Non-Gmo Project Verified, Kosher, & Vegan. If your brand requires any of the listed certifications, our robust Quality Controls, GMP Compliance and Sanitation Program can support them and we will work with you to have all the necessary audits and inspections as required.

HACCP-based food safety planning, supplier approval, environmental monitoring, allergen controls, CAPA/root cause analysis, and internal audits with management reviews.

SQF certification is targeted for Q2 2026, and we’re implementing the SQF Code (Edition 9) for beverage manufacturing now.

We operate with a proactive, risk-based approach aligned with FDA requirements and GFSI standards, specifically SQF.

Quality is built into every step—from raw material receipt to finished goods release, so your product stays consistent, compliant, and protected.

Our plan is developed and managed by PCQIs (Preventive Controls Qualified Individuals) and routinely reviewed and validated.

We comply with 21 CFR Part 117 (cGMP), FSMA Preventive Controls, and HARPC requirements.

Yes, AllBev is an FDA Registered Food Facility.

We use a documented CAPA process with root cause analysis, digital tracking, and defined corrective actions.

We can support trace exercises within hours.

Yes, end-to-end traceability from incoming ingredients through distribution.

It’s our controlled system for SOPs, batch records, real-time monitoring, in-process checks, finished testing, and CAPA management.

Critical equipment is covered under preventive maintenance and calibration programs.

Yes—thermal process controls are managed through HTST pasteurization where applicable.

Through validated process controls, pH verification, critical parameter monitoring, CO₂/gas quality checks, inline filtration, and calibrated measurement systems.

Only after Quality reviews and releases all incoming materials.

Yes, food fraud vulnerability assessments are part of our supplier controls.

With a risk-based program that includes an Approved Supplier List, COA verification, incoming inspections, and traceability checks.

Yes, our environmental monitoring program is based on risk assessment and production zone controls.

A master sanitation schedule, validated cleaning procedures, pre-op inspections, and verification testing (ATP and/or microbiological).

Yes, our environmental monitoring program is based on risk assessment and production zone controls.

A master sanitation schedule, validated cleaning procedures, pre-op inspections, and verification testing (ATP and/or microbiological).

Reach out and we’ll align to your requirements, documentation needs, and expectations upfront.

You get a manufacturing partner built for compliance, audit readiness, and consistent quality.