Medical Devices — Quality Management Systems Undergoing Active Implementation & Certification

To better serve our partners in the medical device, life sciences, and clinical diagnostics sectors, ACI is currently in the process of implementing and achieving ISO 13485 certification.

• Our Commitment: This upcoming certification reflects our transition toward a highly formalized quality management system (QMS) specifically tailored to the medical device industry. We are actively aligning our manufacturing, documentation, and risk-management processes with these rigorous international medical standards.
• The Value to You: Our path to ISO 13485 ensures that we speak the same regulatory language as our medical OEM customers. It guarantees complete traceability, stringent risk assessment, and unmatched process control for critical medical-grade fluidics and precision components.