OBO Precision Blog
Engineering guides for dispensing machines, potting systems, materials, applications, equipment selection, and troubleshooting.
How Should Manufacturers Build a Dispensing SOP Before Production Release?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
How Should FAT and SAT Be Structured for Dispensing Equipment?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
What Defects Should Be Included in a Dispensing Validation Checklist?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
How Should Engineers Validate Potting Processes for Production Stability?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
What Repeatability Data Matters Before Mass Production Launch?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
How Should Buyers Review Pilot Run Data Before Equipment Acceptance?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
How Many Samples Are Enough for Dispensing Process Validation?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
What Acceptance Criteria Should Be Set Before Dispensing Line Release?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated
How Should Manufacturers Validate a Dispensing Process Before Mass Production?
A good sample is not the same thing as a production-ready dispensing process. Validation begins when a team proves that acceptable results can be repeated