Link each production-line non-conformance to its disposition and corrective action, and automatically check subsequent production runs for recurrence.
CAPAs get closed on paper after the root-cause meeting, but nobody systematically checks whether the defect actually stopped recurring in the following weeks of production.
That gap means the same defect can resurface long after everyone believes it's fixed.
capture and link disposition
Investigate and disposition
NC-2291 flags a recurrence of the same weld-porosity defect on Line 2 that CAPA-1187 was supposed to have closed 6 weeks ago. Two units in the last shift's run match the original defect signature.
Try it — same review surface your operators use, with a representative decision. Nothing here is saved or sent anywhere.
Disposition judgment calls, root-cause investigation, and deciding what a recurring defect means for the line, stay with your quality engineers.
See this workflow against your own queue.