Inspection performance
Run agreed good, bad and borderline samples through every approved recipe at representative rates.
Define defects, samples, operating conditions, reject challenges and records before hardware is committed.
Acceptance should challenge the complete decision chain against agreed products, defects, speeds and fault conditions—not simply prove that the camera switches on.
A useful plan starts with a user requirement specification (URS), proves the sensing method with representative samples, checks the built system during factory acceptance testing (FAT), and confirms performance on the production line during site acceptance testing (SAT).
The exact documents and regulated validation route remain the customer’s responsibility unless specifically included in the project scope. Oxford Vision Systems can provide test evidence and validation support appropriate to the supplied system.
Clear requirements reduce quotation assumptions and give later acceptance tests an objective basis.
| Requirement area | Questions to answer | Evidence to supply |
|---|---|---|
| Products and formats | Which packs, sizes, lanes, films, artwork and changeovers are included? | Drawings, samples, SKU list and format range |
| Defect definition | What must fail, at what size or severity, and what can pass? | Labelled good, bad and borderline samples |
| Performance | Required rate, pitch, resolution, coverage, false-reject expectation and miss risk? | Line data, video and current quality records |
| Line interface | Trigger, encoder, PLC signals, ready/fault states, recipes and stop logic? | Electrical drawings, network standard and control philosophy |
| Reject control | How is the pack tracked, removed, confirmed and secured? | Pack behaviour, reject destination and risk assessment inputs |
| Data and users | Which images, counts, events, audit information and access levels are required? | Retention, reporting, backup and user-role requirements |
| Environment | Temperature, washdown, dust, glare, vibration, hygiene and available space? | Site survey, layout and cleaning procedure |
A feasibility study should include production variation, known failures and ambiguous examples. The report should state the setup, sample set, observed separation, limitations and unresolved risks.
Promising laboratory images are not the same as installed performance. Product motion, speed, temperature, lighting isolation and pack presentation have to be included in the engineering basis.
Plan a sample trialFactory acceptance should combine normal operation, known failures and deliberate fault simulation.
Run agreed good, bad and borderline samples through every approved recipe at representative rates.
Challenge consecutive failures, spacing changes, reject confirmation, full-bin and bin-missing conditions.
Verify user access, recipe selection, alarms, counters, image records, data export, backups and recovery.
Site acceptance closes the gap between the build environment and real production.
Verify utilities, guarding, safety functions, line signals, access and physical integration.
Challenge approved products at agreed normal and peak conditions with real operators.
Prove loss of trigger, air, communications, reject confirmation, bin status and other agreed failures.
Complete training, documentation, backups, spares, support and change-control responsibilities.
Routine challenge tests, golden samples, reject checks and change assessment help keep the system within its approved operating space.
Clear, application-led answers before you specify an inspection project.
It should define products and formats, defect classes, minimum relevant feature, line rate, lanes, presentation, recipes, reject response, records, interfaces, environment, user access and acceptance conditions.
A FAT can challenge image acquisition, inspection recipes, known defects, line-rate simulation, tracking, rejection, fault states, data records, access levels, backups and agreed documentation before shipment.
SAT confirms performance after installation with the real line, products, utilities, controls, operators, speeds, changeovers and upstream or downstream interactions.
No. Acceptance applies to the agreed sample space, formats, conditions and criteria. New products, materials or process changes may require assessment, recipe work or revalidation.
A visibly wrinkled seal and a confirmed leaking pack are not interchangeable test samples. A camera may detect a visible feature without establishing leakage, while a leakage path may lack the appearance used by that camera. Label challenge samples by the property that has actually been established so the trial does not claim more than its evidence supports.
For each relevant fault, record how the sample was created and how its expected condition was confirmed. Keep visual appearance, seal strength and package leak integrity as separate attributes where they matter to the product. Agree any supporting test method with the customer's packaging and quality specialists; the appropriate method depends on the pack and the required decision.
Compare the proposed inline result against that independently established reference, including cases where appearance and integrity disagree. Record the sensing method's limitations and which remaining risks are controlled elsewhere. This makes a seal-inspection FAT more informative than demonstrating that obvious marks are rejected. Send actual production faults with their available quality-test results, rather than relying entirely on simulated defects that only change how the seal looks.
No. Appearance, seal strength and leak integrity are distinct properties and need the appropriate evidence.
Record the intended fault, how it was created, how its condition was confirmed and which property the inline system must assess.
Compare seal-inspection methods and limits Define the relevant seal defects
Tell us the pack format, line speed and seal fault you need to detect. We’ll review the application with you.