Loading...

Run: Quality Lab Instrument Calibration Log

Use this Quality Lab Instrument Calibration Log to record calibration dates, traceable standards, as-found/as-left results, and any out-of-tolerance findings...

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 Details

Enter the unique instrument identifier, asset tag, or serial number for the device being calibrated.
Document the instrument name, manufacturer, and model number.
Record the date and time the calibration was performed.
Record the person performing or verifying the calibration.

Calibration Standard and Traceability

Record the calibration standard, reference device, or certified artifact used.
Confirm the reference standard certification or traceability documentation is current and valid.
Confirm traceability is documented to an accepted calibration hierarchy or accredited source, as applicable to the lab's quality system.
Record the procedure, work instruction, or SOP used for the calibration.
Confirm temperature, humidity, vibration, or other required conditions were within the calibration procedure limits during the check.

Calibration Results

Document the instrument condition before adjustment, including any drift or out-of-tolerance observations.
Document the final calibrated condition after adjustment or correction.
Confirm the measured result is within the acceptable tolerance specified by the procedure or manufacturer.
Enter the number of calibration points checked during the verification.
Confirm measurement uncertainty was recorded when required by the calibration method or quality system.

Equipment Status and Non-Conformance

Confirm the instrument displays a current calibration label or equivalent status marking.
Record the next calibration due date or expiration date.
Indicate whether any out-of-tolerance or failed calibration condition was found.
Confirm any potentially affected test results were reviewed for validity and dispositioned per procedure when the instrument was out of tolerance.

Corrective Actions and Approval

Describe repairs, adjustments, retesting, quarantine, or other corrective actions taken for failed or out-of-tolerance items.
Signature of the reviewer approving the calibration record and any required follow-up.
Confirm the record is complete, legible, and suitable for audit review.

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?