Quality inspection and nonconformance
A critical inspection characteristic fails while an earlier supplier issue remains open. How should this lot be handled?
Explore case and packageProduction & quality · Synthetic business case
Quality traceability and corrective actions
Can a customer return be traced back to material, process and equipment evidence?
Trace material batches through operations, inspections, defects and complaints to review quality evidence and corrective/preventive actions.
For · Quality management, production engineering and customer quality teams
Your path after importing
Follow the process. Check each step.
This is a walkthrough for the product. The page describes the case; calculations and business actions run inside your DataFocus project.
- 01
Inspect the business records
Inspect a material batch and its process, inspection and customer-complaint records.
- 02
Analyze and check the evidence
Run the quality analysis and check batch links, defect severity and equipment alarms against the source rules.
- 03
Change an input and recalculate
Edit the material source record and recalculate to compare the quality assessment and response.
- 04
Review actions and their records
Review the current response using the guide, then inspect corrective tasks, knowledge cases and audit records.
Business context
Bring data, knowledge and actions together.
Use these business objects to understand the case. After importing, inspect the fields, relationships and rules, then adapt them to your work.
- Material batches
- Process records
- Inspection lots
- Defect events
- Customer complaints
View package resources33 resources
- Business panels
- 1
- Documents
- 3
- Execution definitions
- 1
- Forms
- 11
- Knowledge resources
- 1
- Ontologies
- 1
- Relationships
- 4
- Tables
- 11
From a demo to your business
Bring a concrete question to the next conversation.
Confirm these differences before choosing the data to connect and the rules to retain. Example data and objects do not automatically connect to your production systems.
- Preserve batch links across materials, work in progress, inspections and returns.
- Define defect severity, isolation scope and corrective-action closure criteria.
- Map quality-release and production-response responsibilities; validate live production changes separately.