Current condition
Identify the can and end references, supplier and batch, approved tooling and setup used for each sample. Record the filled-can condition, seam examination method and the result obtained.

What evidence should be agreed before acceptance testing for can seaming equipment?
Agree the can and end references, representative filled cans, approved tooling, seam examination method and acceptance limits before the equipment trial. Record who is responsible for reviewing the results.
Include normal production, difficult component or fill conditions, changeovers and fault recovery. Keep setup and first-pack records linked to the samples and agree how unacceptable packs will be handled.
Plan can seaming equipment around your product, pack range, target output, cleaning needs and finished-pack checks. Discuss a practical line concept with Lancing using representative samples. Use this guide to resolve finished-pack checks and reject handling before it limits the final system.
Discuss your application

Identify the can and end references, supplier and batch, approved tooling and setup used for each sample. Record the filled-can condition, seam examination method and the result obtained.
Include the planned can-and-end combinations, representative filled cans and known difficult samples. Cover the intended production pattern and the changes that require a fresh setup or first-pack check.
Link the results to the agreed acceptance limits and identify who reviews them. Record the required response to a failed seam check, including the handling of affected packs and the checks before production resumes.
Keep the can and end references, supplier batch and filled-can condition with the trial samples. Record the condition at closing that the results represent.
List every can-and-end combination to be included, with its approved tooling and setup reference. State which formats and changes the trial has actually covered.
Agree the examination method and acceptance limits with the responsible packaging and quality team. Retain the setup and first-pack records alongside the results.
Record the intended production pattern, agreed trial conditions and accepted output. Include replenishment, checks, interruptions and recovery when judging the complete operating cycle.
Include the cleaning, access and format-change tasks in the agreed trial. Record how the setup is restored and how the first packs are checked before normal production resumes.
Define how failed results and unacceptable packs are identified, recorded and handled. Agree who reviews them and the response required before the result is accepted.