Whenever I help a client prepare for Stage 2, I remind them that this is the real audit—the moment when auditors step onto the production floor, talk to your team, review your records, and confirm whether your food-safety system works in everyday practice. Stage 1 checks structure; Stage 2 checks reality.
Here’s what most companies worry about: “Do we have enough monitoring records?” “Will our staff know how to answer questions?” “What if the auditor finds gaps in our HACCP plan?”
This checklist breaks everything down into practical steps. It shows you what auditors expect, what evidence you need ready, where companies usually slip up, and how to walk into the audit confident and prepared. Everything here comes from real audits I’ve supported—across manufacturers, processors, distributors, and catering businesses.
Now that we’ve set expectations, let’s walk through each part of the Stage 2 checklist one section at a time.
Understanding ISO 22000 Stage 2 Audit Requirements (Operational Compliance Review)
Here’s what I’ve noticed over the years: many teams assume that if Stage 1 went well, Stage 2 will be just as smooth. But Stage 2 is where auditors validate the effectiveness of your entire FSMS—live, in real time.
Stage 2 focuses heavily on:
How you run your processes
How you monitor hazards
Whether your records reflect consistent implementation
How well your team understands their responsibilities
Whether your controls truly prevent contamination
Auditors follow your process flow step by step. If your hazard analysis says there’s a CCP at cooking, they’ll go straight to that area and verify monitoring logs, operator competence, equipment calibration, and corrective actions.
Pro Tip: Match your operational practice to your documented HACCP plan. Auditors instantly notice when they don’t align.
Common Pitfall: Assuming auditors will accept “we do it, but we forgot to record it.” Missing records count as missing controls.
Stage 2 Pre-Audit Essentials Checklist (Evidence You Must Have Ready)
Before the audit even starts, auditors want to see proof that your system has been operating consistently. That usually means at least 3–6 months of complete records.
Make sure you have evidence for:
CCP/OPRP monitoring
Verification and validation
PRP implementation
Calibration and equipment maintenance
Traceability tests
Corrective actions and CAPA
Internal audit results
Management review decisions
Supplier approval and material inspections
I once worked with a beverage manufacturer who had a flawless HACCP plan, but their CCP logs had inconsistent entries. The auditor paused the audit for an hour while they searched for missing data. It didn’t cause a failure, but it created a stressful situation that was completely avoidable.
Pro Tip: Create a single digital or printed folder titled “Stage 2 Audit Evidence Pack.” Keep everything indexed and ready.
Common Pitfall: Records with gaps, missing signatures, or inconsistent monitoring times.
Production Floor Readiness Checklist (Walkthrough Expectations)
Stage 2 includes a thorough walkthrough. Auditors look at everything—hygiene, workflows, equipment condition, material flow, and food-safety culture in action.
Key areas they inspect:
Personnel hygiene and handwashing practices
Allergen segregation
Cleaning tools and chemical storage
Pest-control devices and documentation
Equipment hygiene and maintenance status
Storage conditions and temperature control
FIFO and stock rotation
Waste handling and foreign-body prevention
Layout and cross-contamination risks
This part often reveals surprises. A client once had impeccable documentation but forgot to replace a damaged sieve in one area. The auditor spotted it immediately. It didn’t derail certification, but it became a minor nonconformity that required repair and evidence of correction.
Pro Tip: Do your own walkthrough the day before, following the same route the auditor will take.
Common Pitfall: Unlabeled containers, expired cleaning logs, or clutter in high-risk zones.
CCP, OPRP & HACCP Plan Verification Checklist (Core of Stage 2 Audit)
Your CCPs and OPRPs are the heart of the audit. Auditors want to see that your controls actually work and that your team can demonstrate how they manage hazards.
Expect auditors to check:
How you identified CCPs/OPRPs
Whether monitoring frequency matches the HACCP plan
Corrective actions taken when limits were exceeded
Validation evidence
Verification activities and trend analysis
Operator competence at each point
Calibration of instruments used in monitoring
Here’s an example: a ready-to-eat processor I helped had a CCP for metal detection. The operator knew the routine but froze when the auditor asked him why it was critical. After a quick reset, he explained it clearly. The auditor appreciated the honesty—but it showed the importance of confidence and understanding, not memorization.
Pro Tip: Ask operators to explain their steps in their own words during prep sessions.
Common Pitfall: Monitoring logs that don’t match the documented procedure.
Team Competence & Training Checklist (Interview Readiness)
Auditor interviews aren’t designed to intimidate your team—they’re meant to confirm that your FSMS is truly understood by the people doing the work.
Auditors typically ask operators:
What hazards they handle
How they monitor a CCP or OPRP
What they do when limits aren’t met
How they document their activities
Where procedures are located
How they report issues
A simple, confident answer often impresses auditors more than textbook knowledge. In one facility, an operator explained his CCP monitoring by describing his exact daily routine. It was clear, practical, and aligned with the procedure—perfect.
Pro Tip: Do short “audit readiness huddles” with staff a few days before the audit.
Common Pitfall: Staff relying on technical terms they don’t fully understand.
Traceability and recall are non-negotiable. If your system can’t trace a product back through raw materials, packaging, and processes within a few hours, auditors will raise a major concern.
Auditors check:
Forward and backward traceability
Mock recall results and timelines
Emergency response training
Incident logs and corrective actions
Pro Tip: Conduct a mini traceability trial the week before the audit to ensure everyone remembers the process.
Common Pitfall: Incomplete tracking of packaging materials or subcontracted processes.
Auditors want to see how your organization handles problems—not just how you prevent them.
Evidence should show:
Clear root-cause analysis
Practical corrective actions
Verification of effectiveness
Trends in deviations, complaints, downtime, rework
Documented improvements
One company I worked with created a simple Excel dashboard showing complaint trends and how they reduced foreign-body incidents. The auditor highlighted it as an example of strong continual improvement.
Pro Tip: Keep your CAPA system simple but consistent. Complexity leads to errors.
Common Pitfall: Closing corrective actions without verifying whether they worked.
Legal & Regulatory Compliance Checklist
Stage 2 auditors check your understanding of food-safety regulations and how you maintain compliance.
Expect to present:
A regulatory register
Procedures for monitoring regulatory updates
Licenses and permits
Labeling and allergen compliance evidence
Supplier regulatory documentation
Pro Tip: Keep a dated log of regulatory changes you’ve reviewed—even simple notes show active monitoring.
Common Pitfall: Outdated permits or missing allergen-labeling checks for suppliers.
Stage 2 Audit Day Logistics & Presentation Checklist
A well-organized audit day signals confidence and competence.
Prepare:
An agenda for the day
Access to your FSMS Index
Availability of key staff
A prepared walkthrough route
Opening and closing meeting notes
A central audit coordinator
Pro Tip: Keep documents visible and easy to access. Smooth document retrieval builds trust quickly.
Common Pitfall: Only one person knows where documents are stored, causing delays and awkward moments.
FAQs
How much evidence do we need for Stage 2?
Most certification bodies expect at least 3–6 months of consistent, complete records.
What causes most Stage 2 nonconformities?
Gaps between actual practice and documented procedures, weak CCP/OPRP monitoring, or lack of PRP implementation.
Do auditors always interview operators?
Yes. Operator competence is central to evaluating FSMS effectiveness.
Conclusion: Your Clear Roadmap to Passing Stage 2 with Confidence
Stage 2 is where your food-safety system proves itself. When your records are complete, your team is confident, and your operations reflect your documented controls, the audit flows smoothly. I’ve seen companies of all sizes succeed because they focused on consistency, clarity, and readiness—not perfection.
Use this checklist as your guide, and you’ll walk into the audit prepared, structured, and in control.
Melissa Lavaro is a seasoned ISO consultant and an enthusiastic advocate for quality management standards. With a rich experience in conducting audits and providing consultancy services, Melissa specializes in helping organizations implement and adapt to ISO standards. Her passion for quality management is evident in her hands-on approach and deep understanding of the regulatory frameworks. Melissa’s expertise and energetic commitment make her a sought-after consultant, dedicated to elevating organizational compliance and performance through practical, insightful guidance.