Certifications

POA's Quality Management System is independently certified to ISO 9001:2015 standards—the international benchmark for quality management.

This proves we have documented processes, continuous improvement systems, and quality controls throughout our organization. Our customers benefit from consistent service delivery and complete documentation.

Working with an ISO-certified partner means predictable outcomes, comprehensive documentation packages, and the confidence that our processes meet regulatory expectations.

POA is certified to manufacture Underwriters Laboratories (UL) Listed industrial control panels under the UL508A standard for general purpose installations.

UL508A certification ensures our control panels are designed and built to prevent electrical hazards, meet code requirements, and pass authority having jurisdiction (AHJ) inspections.

UL-listed panels eliminate inspection delays, reduce liability concerns, satisfy insurance requirements, and provide documented proof your electrical systems meet industry standards.

POA is certified to manufacture UL698A Listed control panels with intrinsically safe circuits for monitoring and controlling equipment in hazardous classified locations.

Hazardous location control systems require specialized design, construction, and documentation to prevent ignition sources in classified areas.

Properly certified hazardous location panels protect workers, satisfy OSHA requirements, pass code inspections, and reduce liability in high-risk environments.

POA's calibration services are traceable to the National Institute of Standards and Technology (NIST)—the United States' primary standards laboratory.

NIST traceability proves the accuracy of calibrated instruments through an unbroken chain of comparisons to national standards. This traceability is required by FDA, ISO, and other regulatory bodies..

NIST-traceable calibration certificates satisfy regulatory requirements and provide documented proof your measuring and monitoring instruments deliver reliable data throughout their calibration intervals.

POA's asset management services comply with FDA 21CFR Part 11 requirements for electronic records and electronic signatures.

FDA-regulated industries require electronic systems that maintain data integrity, prevent unauthorized changes, and provide complete audit trails.

Compliant asset management systems simplify FDA inspections, eliminate manual record-keeping errors, and ensure your calibration and validation documentation meets regulatory expectations.