Dear Saferpakers,
ISO 22000 requires you to establish procedures and documentations to handle nonconformity products derived from out-of-range or defective monitoring devices / equipment.
The international standard also requires you to do more than just that. It expects you to review and if necessary, hold, isolate and investigate all previous production batches (released later if justified) that were suspected to have been monitored under the "out-of-range or defective devices/equipment"
Handling of nonconformity product is a huge area of concenr under ISO 22K. Have you got this Covered?
Regards
Charles Chew
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