Run Glucometer Cleaning and QC Verification — Free

Device Identification and Readiness

Glucometer identified by asset ID or serial number

Record the device identifier for the glucometer being inspected.

Device present, intact, and powered on critical (required)

Confirm the meter is available for use, with no visible damage and functional power status.

Yes No N/A

Test strip lot and expiration verified critical (required)

Verify the current strip lot is within expiration and matches the approved product in use.

Yes No N/A

Control solution lot and expiration verified critical (required)

Confirm control solution is within expiration and approved for the device.

Yes No N/A

Cleaning and Disinfection Verification

Exterior surfaces cleaned with approved disinfectant wipe critical (required)

All external surfaces were cleaned using a fresh disinfectant wipe per manufacturer instructions for use (IFU).

Yes No N/A

Required contact time observed critical (required)

Disinfectant remained wet for the full manufacturer-specified contact time.

Yes No N/A

Meter free of visible soil, residue, or contamination critical (required)

Inspect the device housing, buttons, screen, and strip port for visible debris or residue.

Yes No N/A

Cleaning supplies available and in date

Approved disinfectant wipes and related supplies are available, labeled, and not expired.

Yes No N/A

Quality Control Testing

QC level 1 result within acceptable range critical (required)

Document whether the first control level result falls within the manufacturer-accepted range.

Yes No N/A

QC level 2 result within acceptable range critical (required)

Document whether the second control level result falls within the manufacturer-accepted range, if required by the device or policy.

Yes No N/A

QC results documented with date, time, and operator critical (required)

Verify QC documentation includes date, time, operator identification, meter ID, strip lot, and control lot.

Yes No N/A

Out-of-range QC investigated and meter removed from service if needed critical (required)

If any QC result is out of range, confirm the device was taken out of service and escalation was initiated per SOP.

Yes No N/A

Documentation and Compliance

Inspection completed by authorized staff member critical (required)

Inspector attests that the daily cleaning and QC verification was completed accurately.

Non-conformances and corrective actions documented

Record any deficiencies, corrective actions, notifications, or device hold status.

Reference to CLIA and manufacturer requirements followed critical (required)

Confirm the inspection was completed in accordance with applicable CLIA requirements and the glucometer manufacturer IFU.

Yes No N/A

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Run: Glucometer Cleaning and QC Verification

Device Identification and Readiness

Cleaning and Disinfection Verification

Quality Control Testing

Documentation and Compliance

Get your results