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Supplier Audit Checklist for the Food Industry

Your products are only as safe as the raw materials and packaging that go into them. Certificates and questionnaires tell you a lot about a supplier, but sometimes you need to see the site for yourself. This guide explains when a supplier audit is worth doing, what to check and how to turn findings into an approval decision. The full checklist is a free download.

Supplier Audit Checklist for the Food Industry

What Is a Food Supplier Audit?

A food supplier audit is an on site or remote assessment of a supplier's food safety and quality controls against your requirements. Alongside risk assessment, certificates and document review, it helps you decide whether to approve a supplier and how closely to monitor them afterwards.

In the US, onsite audits are one of the supplier verification activities listed in 21 CFR 117.410(b): "(1) Onsite audits; (2) Sampling and testing ...; (3) Review of the supplier's relevant food safety records; (4) Other appropriate supplier verification activities". A supply chain program must cover approved suppliers (117.420), determining verification activities (117.425), conducting them (117.430 and 117.435) and documenting them (117.475). Verification is required "before using the raw material ... and periodically thereafter" (117.430(a)).

When to Audit a Supplier (Risk Based Approach)

Not every supplier needs a visit. Use your supplier risk assessment to decide:

  • Higher risk: raw materials with significant hazards, suppliers without a recognized certificate, poor history or recent incidents. Consider an audit.
  • Medium risk: suppliers holding a GFSI benchmarked certificate, with occasional issues. Document review and questionnaires may be enough, with an audit if concerns arise.
  • Lower risk: suppliers holding a GFSI benchmarked certificate, supplying low risk materials with a good record. Monitor certificates and performance.

For US facilities, where a hazard in a raw material will be controlled by the supplier and there is a reasonable probability that exposure will result in serious adverse health consequences or death, the appropriate verification activity is an onsite audit before first use and at least annually, unless a written determination says other activities or less frequent audits give adequate assurance (21 CFR 117.430(b)(1) and (b)(2)).

Supplier Audit Checklist: Sections and Questions

Supplier Audit Checklist: Sections and Questions
SectionSample Questions
Food Safety SystemIs there a current HACCP or food safety plan, reviewed and signed off?
CertificationWhich standard is the site's certificate issued against, what is the scope and when does it expire?
Premises and HygieneAre the building, equipment and cleaning in good condition and controlled?
Allergen ControlIs there an allergen risk assessment, with segregation and validated cleaning?
Pest ControlIs there a contracted program with current records and trend reviews?
TraceabilityCan the supplier trace a batch back to its raw materials and forward to customers? See our recall and traceability guide and, for US supply, our FSMA 204 guide.
Foreign Body ControlAre glass, metal and hard plastic controlled, with detection where appropriate?
SpecificationsAre specifications agreed and current for the materials you buy?
Staff and HygieneAre hygiene rules followed, and is food safety training recorded?
Corrective ActionsAre nonconformances closed with root cause analysis?
Food Defense and FraudAre there TACCP and VACCP assessments for the site?
Primority manages supplier records, documents and approvals. Request a Demo

Scoring Findings and Setting Approval Status

Scoring Findings and Setting Approval Status
FindingMeaningTypical Outcome
CriticalDirect risk to food safety or legalityDo not approve, or suspend
MajorSignificant failure of a controlConditional approval pending corrective action
MinorIsolated lapse with no immediate riskApprove, with corrective action

Set the approval status from the overall result: approved, conditionally approved or not approved. This grading is a common convention; align it with your own procedure.

Following Up Nonconformances

  1. Agree each nonconformance with the supplier at the closing meeting.
  2. Ask for root cause analysis and a corrective action plan with dates.
  3. Review the evidence and verify each fix.
  4. Update the supplier's approval status and risk score.
  5. Record everything, as auditors will ask to see it.

If you also audit against a certification standard, our IFS Food Version 8 checklist covers the requirement areas auditors look at.

Download the Checklist

Get the full editable supplier audit checklist, with every section, scoring guidance and a corrective action log.

FAQs

What is a supplier audit in the food industry?

A supplier audit is an assessment of a supplier's food safety and quality controls against your requirements. It can be on site or remote, and sits alongside certificates, questionnaires and risk assessment in supplier approval.

How often should food suppliers be audited?

Audit frequency should follow risk. Under US rules, suppliers controlling serious hazards need an onsite audit before first use and at least annually, unless a written determination says otherwise; lower risk suppliers can be verified periodically through other activities.

Can a GFSI benchmarked certificate replace a supplier audit?

It depends on the risk, and you remain responsible for verification. US rules allow verification activities other than onsite audits based on supplier performance and risk, except for serious hazards, which need an annual onsite audit unless a written determination says otherwise.

Talk to the Primority Team

Primority's supplier quality management software helps food manufacturers approve suppliers, send questionnaires, collect supplier documents, track certificate expiry and score supplier risk in one place, trusted since 2010.

For on site work, see the Primority Audit App.

Request a Demo