Corrective actions are part of every BRC V9 journey. Even strong, well-managed sites receive findings. After supporting multiple facilities through BRC audits, I’ve seen the same uncertainty appear once the closing meeting ends:
“What exactly do we submit? How detailed should it be? And how do we avoid repeat findings next year?”
Responding correctly isn’t just about fixing an issue — it’s about showing the certification body that your system can identify, control, and prevent failures over time. That’s what gives auditors confidence, and that’s ultimately what protects your brand and certification status.
This guide walks you step-by-step through understanding findings, responding effectively, writing strong corrective actions, submitting evidence, and building systems to prevent recurrence.
Understanding BRC V9 Non-Conformity Grades (Minor, Major & Critical)
During the closing meeting, findings are classified into categories — and the severity directly affects timelines, expectations, and sometimes certificate status.
Here’s a quick breakdown:
Minor Non-Conformity A requirement is partly met, or documentation/practice doesn’t fully align — but there’s no direct food-safety or legality risk.
Major Non-Conformity A requirement isn’t met in a way that could impact food safety, legality, or integrity.
Critical Non-Conformity A serious situation where food safety, legality, or product integrity is compromised. This can lead to immediate certification suspension.
The grading isn’t meant to be punitive — it’s a structured way of prioritizing risk.
Pro Tip: Treat every non-conformity seriously. Even minor findings can escalate in later years if they repeat.
A common misconception is thinking a minor issue isn’t urgent. The truth is: repeat minors are one of the fastest ways to damage audit confidence.
Root Cause Analysis (RCA) for BRC V9 Findings — Getting Beyond Symptoms
A corrective action response begins with root cause analysis. Certification bodies want to see that you understand why the issue occurred — not just that you’ve corrected it.
Useful tools include:
The 5 Why’s
Fishbone (Ishikawa) Diagram
Barrier or system analysis
A strong root cause focuses on the system, not the individual. “Operator error” rarely satisfies an auditor unless it’s clear why the oversight happened — lack of clarity, training gaps, poor supervision, unclear expectation, or systemic weakness.
Pro Tip: Your analysis should answer one core question: “What failed in the system that allowed this finding to occur?”
A small example: A missed metal detector check isn’t just a missed check — it may indicate gaps in training, unclear accountability, or ineffective oversight.
Once the root cause is clear, build your corrective action response. A solid format helps:
Restate the finding clearly
Describe the immediate fix (correction)
Explain the root cause
Define longer-term corrective action
Explain how effectiveness will be monitored
A strong response is calm, factual, and concise.
Pro Tip: Avoid defensive wording. Auditors aren’t looking for excuses — they’re assessing system maturity and accountability.
A common pitfall is only fixing the symptom. Updating a record without updating a procedure or retraining staff rarely solves anything long-term.
Evidence Submission & Documentation (What the Auditor Expects to See)
Certification bodies need proof that corrective actions are completed and effective. This evidence may include:
Revised procedures
Updated forms or logs
Training records with attendance and competency validation
Photos or records showing the correction
CAPA tracking logs
Internal audit verification
How you present evidence matters. Organized submissions signal reliability and system control.
Pro Tip: Use labelled folders or a structured PDF with a clear index — make it easy to review.
Sending everything you can find in panic mode doesn’t help. Clear, targeted evidence always performs better.
Monitoring Effectiveness & Preventing Recurrence (Closing the Loop)
Corrective action doesn’t end when documents are uploaded. The site must show the improvement is lasting.
This can be done through:
Follow-up checks
Trending data
Internal audit verification
Management review updates
Performance metrics
Effectiveness reviews are often performed at 30, 60, and 90 days depending on the risk level.
Pro Tip: Treat trend analysis as early warning — not a report card.
One facility identified a slow increase in hand-washing non-compliances. Because they monitored proactively, they updated training before it became an audit finding the following year.
Building a Continuous Improvement System (Not Just Fixing Findings)
Strong corrective actions feed back into the system and strengthen:
Risk assessments
HACCP decisions
PRPs
SOPs
Training programs
Supplier controls
Culture maturity
Sites that handle findings well typically see fewer repeated issues and smoother audits over time.
Pro Tip: Create a corrective-action lessons-learned log. It helps avoid repeated problems — especially during staff turnover.
Q1: How fast do we need to submit corrective actions? Certification bodies typically expect submission within a defined timeframe (often 28 days), so planning and ownership are important.
Q2: Can a minor non-conformity become a major next year? Yes — repeated minors often indicate weak corrective action or ineffective system controls.
Q3: Can templates be used? Yes — but the content must reflect actual site conditions. Auditors can immediately tell when responses are generic.
Conclusion: Responding to Findings With Professionalism & Structure
Corrective actions aren’t about proving perfection — they’re about proving control. When your responses are structured, root cause is clear, evidence is organized, and actions prevent recurrence, certification bodies gain confidence in your system.
If you’d like help reviewing a response before submission or creating a reusable corrective-action framework, I can build one based on your risk level and audit history.
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.