QUALITY AND TRACEABILITY

Find the records for the batch under investigation.

Relate the affected output to recorded operating conditions and available inspection results.

When a nonconformity occurs, the first challenge may be establishing when and under what conditions the product was manufactured. Process data are useful when linked to the correct batch, cycle or time interval.

QUALITY / MANUFACTURING RECORDS

Investigating a nonconformity requires preserving batch context.

Traceability is established when batch identifiers, measured conditions and inspections are linked by verifiable dates and product references.

KERN MONITOR history screen with recorded injection-pressure curves.
KERN IoP interface displaying recorded process variables. Interface shown in Spanish.

IDENTIFY

Batch, work order, product, mould and production period.

REVIEW

Variables actually measured during the period being investigated.

COMPARE

Inspection results and documented process changes.

What can be analysed?

KERN MONITOR demonstration displaying injection-pressure curves.
Process demonstration with KERN IoP instrumentation. Interface shown in Spanish.

01

Production identification

Define how work orders, products, moulds, materials and machines are linked. The level of detail depends on the identifiers actually captured.


02

Process variables and inspection

Select process variables relevant to the defect being investigated. Retain inspection results, timestamps and acceptance criteria.


03

Review the affected period

Review events and operating conditions within the identified interval. Correlations may guide the investigation, but further verification is required to establish a cause.

QUALITY · FURTHER INVESTIGATION

How can rejects be recorded during production?

Reject counts are meaningful when associated with the product, relevant time interval and inspection criteria. Operators can record good and rejected parts through SMARTPRO at the machine, including defect categories when configured.

SMARTPRO quality-reporting form with rejected-part counts.
Interface shown in Spanish.

What information does quality assurance need?

Defining inspection times, quantities, order or batch identifiers and recording frequency helps relate results to process data. Recorded quality information can contribute to OEE monitoring during the shift.

Further questions: Explore the SMARTPRO form · Link batches to operating conditions · Understand the other OEE losses

A PLANT-FLOOR EXAMPLE

Before drawing conclusions.

If records identify a batch and time interval, the relevant context can be reconstructed. Claiming part-level traceability requires a persistent identifier across inspection and other applicable operations.

RELATED CONTENT

Process conditions

Variables and quality results.

Engineering

Preparing an engineering investigation.

TO INVESTIGATE FURTHER

Compare manufacturing conditions and quality results

Document machine, material, mould, product and inspection results before attributing quality variation to the process.

Read the technical guide →

APPLICATION ASSESSMENT

Review a traceability case

Agree on minimum data fields: production identifier, equipment, timestamp, measured variable and source, inspection results and person responsible for recording. Data retention, access and export are specified for the project.

Describe your needs using the information available. Confidential attachments are not required.

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PM Tec Engineering, through its Industry 4.0 division, KERN IoP.
Cota, Cundinamarca · Colombia.

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