WORLD CLASS QUALITY ASSURANCE AND LEAN MANUFACTURING

Each Pentair Technical Products manufacturing facility worldwide meets ISO Global 9001 2000 registration requirements. Every system, case, cabinet and component is fully inspected before it is released for production under the strict guidelines of our Advanced Product Qualification Process. Extensive process control and monitoring capabilities include the use of coordinate measuring machines, torque testing and hardness testing equipment, coating thickness and color testing systems, and other precision measuring instruments to detect process variability. Lean manufacturing techniques such as Value Stream Mapping, Kaisen, One Piece Flow and Total Productive Maintenance assure you that there are no unnecessary manufacturing costs for your medical electronic enclosure.

Our in-house compliance testing is unmatched in the industry with UL approved test labs, EMC, CSA/TUV, water and salt spray, UV, and static load testing facilities. Included in Pentair's design verification and test procedures is thermal and airflow management analysis for each customer's enclosure. We guarantee that your electronic packaging solutions meet or exceed all applicable industry performance standards and your specifications.

Variety of cabinets to
shield and protect sensitive
electronic equipment