Loading...

Run: Vacuum Decay Leak Test Log

Vacuum Decay Leak Test Log for recording package integrity results, setup parameters, and pass/fail decisions under ASTM F2338. Use it to document non-destru...

Fill this out, get a PDF emailed to you. No account required. Want to run it with your team and track results? Sign up free →

Inspection Identification

Record the product name, lot/batch number, sample ID, and any packaging configuration identifiers.
Capture the date and time the vacuum decay leak test was performed.
Record the inspector or operator performing the test and their qualification or authorization status.
Confirm the test is being performed as a non-destructive vacuum decay leak test aligned to ASTM F2338.

Test Equipment and Calibration

Record the instrument model, serial number, and chamber or fixture identification used for the test.
Confirm calibration is current for the test instrument and any connected pressure or vacuum sensors.
Verify the chamber, gaskets, O-rings, fittings, and seals are clean and in serviceable condition before testing.
Confirm any required reference standard, positive control, or challenge sample is available and identified per site procedure.

Test Setup and Parameters

Enter the number of packages or samples tested in this log entry.
Record the target vacuum level used for the test.
Record the vacuum hold duration used for the test.
Record the chamber or ambient temperature at the time of testing if required by the method or SOP.
Record the pass/fail criteria, including allowable leak threshold or instrument decision limit used for this test run.

Vacuum Decay Results

Confirm the measured vacuum decay result is within the documented acceptance criteria.
Enter the measured decay value observed during the test.
Indicate whether the instrument or operator observed evidence of a leak, unstable pressure trend, or abnormal decay pattern.
Confirm repeat runs, if performed, were consistent with the original result and within site-defined repeatability limits.

Defects, Disposition, and Sign-Off

Record whether any failed, borderline, or suspect samples were identified and routed to the appropriate disposition process.
Enter the CAPA, deviation, investigation, or hold reference number when a failure or non-conformance occurs.
Signature of the person completing the log entry.
Confirm review and approval by supervisor, QA, or designated reviewer when required by site procedure.

Get your results

Enter your email — we'll send you a PDF of your filled-out template, plus the occasional MangoScoop newsletter (templates, workflow tips, product updates). Unsubscribe anytime — link is in every email.

Generated with MangoApps Templates — browse 250+ free
Ask AI Product Advisor

Hi! I'm the MangoApps Product Advisor. I can help you with:

  • Understanding our 40+ workplace apps
  • Finding the right solution for your needs
  • Answering questions about pricing and features
  • Pointing you to free tools you can try right now

What would you like to know?