This checklist is designed to evaluate and qualify test laboratories involved in counterfeit electronic part detection and analysis, ensuring compliance with the SAE AS5553 standard for the aerospace and defense industry.
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About This Checklist
The SAE AS5553 Test Laboratory Evaluation Checklist is an essential tool for aerospace and defense industry professionals to assess and qualify laboratories involved in the detection and analysis of counterfeit electronic parts. This comprehensive checklist aligns with the SAE AS5553 standard, focusing on the capabilities, procedures, and quality management systems of test laboratories. By implementing this checklist, organizations can ensure they partner with competent laboratories, enhancing their ability to detect counterfeit components and maintain compliance with industry regulations.
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Select compliance status.
Enter a percentage value.
Provide details of the calibration procedure.
Select the date of the last validation.
Select the maintenance status.
Provide a detailed description of any anomalies.
Select the status of the quality control process.
Enter a percentage value.
Provide a detailed description of corrective actions.
Select the date of the last audit.
Provide an overview of training records.
Select the frequency of internal reviews.
Select the certification status.
Provide a detailed description of the improvement plan.
Enter a percentage value.
Select the date of the last audit.
Select the status of the corrective action process.
Enter any relevant comments.
Select the certification status.
Enter a percentage value.
Provide a detailed description of traceability procedures.
Select the date of the last audit.
Select the status of the non-conformance handling process.
Enter any relevant feedback.
FAQs
Evaluating test laboratories is crucial because it ensures that the facilities responsible for detecting and analyzing potential counterfeit parts have the necessary expertise, equipment, and procedures to provide accurate and reliable results, which is fundamental to effective counterfeit prevention.
The checklist covers areas such as laboratory accreditation, technical competence of personnel, testing equipment calibration and maintenance, test method validation, quality management systems, and reporting procedures.
Initial evaluations should be conducted before engaging a new laboratory, with follow-up assessments performed annually or more frequently if there are significant changes in the laboratory's operations, personnel, or equipment.
The evaluation process should involve quality assurance managers, technical experts familiar with counterfeit detection methods, and procurement specialists. In some cases, third-party auditors with specific expertise in laboratory assessment may also be engaged.
This checklist includes items to verify the laboratory's proficiency testing participation, inter-laboratory comparison results, internal quality control procedures, and the traceability of measurements to national or international standards, all of which contribute to result reliability.
Benefits
Ensures selection of qualified and capable test laboratories
Enhances reliability of counterfeit detection and analysis results
Supports compliance with SAE AS5553 laboratory requirements
Reduces risks associated with undetected counterfeit parts
Improves overall quality assurance in the supply chain