Audit Pitfalls and Recommendations
Recommendations
- Run your own food safety system & learn to validate, audit, defend it!
- Accurate information presented to audit companies equals more audit value
Documentation Requirements
- Staff cannot access/unaware of required documentation
- Documents inadequately controlled, e.g. no approval, outdated/obsolete documents, inconsistent versions
- Relevant documents of external Origin not identified, e.g. food regulations, customer specification, standards etc.
- Distribution of external documents not controlled
- Improper data correction -obliterated/erased data or liquid paper
Management Responsibility/Resource Management
- Commitment statement does not mention conformity to legal, regulatory & customer food safety requirements.
- Review documentation does not detail inputs/outputs; objectives not measurable or not tracked
- Communication procedures not in place/not effective; personnel to communicate with external parties not defined
- Food safety issues/changes not communicated to food safety team promptly
- Emergency preparedness/business continuity plans not in place or not tested annually
- Staff/back up personnel training/evaluation not documented
- No review of competence for outsourced activities
Processing/Product Realization
- PRPs not in accordance with PAS 220 or not well documented
- Supplier review for hazard controls not documented
- Food safety team/meetings not documented
- Insufficient information on raw material characteristics to conduct hazard analysis
- Product descriptions/end product characteristics incomplete
- Process flow diagrams/plant schematics not accurate or missing steps like water treatment, waste & rework
- Food Safety hazards reasonably expected to occur not identified
- Control measures for hazards identified not adequately defined
- Hazard assessment/prioritization not adequate
- CCPs not logically determined or not capable of being monitored
- Information required for OPRPs (FSSC 22000) or HACCP plans not adequately defined e.g. inaccurate critical limit, incomplete monitoring procedure, correction and corrective action not clearly defined
- Incomplete corrective action documentation or no segregation/identification/safe disposition of affected product
- Missing informationl1ests for traceability from raw materials through in process/finished product to next level of distribution
Validation, Calibration, Verification, Continual Improvement
- HACCP/OPRP plans not validated or not properly documented
- Key measuring equipment not calibrated at least annually
- Internal audit not carried out at least annually or all standard requirements were not covered
- Internal auditors not consistent or not trained
- Corrective action not performed in response to internal audit non-conformities or not verified to be effective
- Results not analyzed to confirm overall effectiveness of FSMS & identified opportunities for improvement/updating