People Matter At Avada
Curabitur aliquet quam id dui posuere blandit. Quisque velit nisi, pretium ut lacinia in, elementum id enim. Donec sollicitudin molestie malesuada.
A Place Where People Enjoy Working.
Quisque blandit dolor risus, sed dapibus dui facilisis sed. Donec eu porta elit. Aliquam porta sollicitudin ante.
Core Hiring Principles
Curabitur aliquet quam id dui posuere blandit. Quisque velit nisi, pretium ut lacinia in, elementum id enim. Donec sollicitudin molestie malesuada.
We are pleased to inform you that we have successfully passed the audit and be certified with ISO 13485:2016.
We are pleased to inform you that we have successfully passed the audit and be certified with ISO 13485:2016.
We are pleased to inform you that we have successfully passed the audit and be certified with ISO 13485:2016.
In 2020, in order to better provide customers with compliant and efficient PCBA services for medical equipment, ABP established a quality management system covering the entire service process of medical products, and passed the on-site audit in November 2020.
ISO 13485:2016 is the standard for a Quality Management System for the design and manufacture of Medical Devices. “ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met the requirements in ISO 13485. The successful passing of ISO13485 means that ABP’s quality management has reached international standards. This is not only an affirmation of ABP’s existing management system, but also an important milestone in the development process.
In the future, ABP Electronics Limited will take the international management level as the basic guarantee, and is committed to providing customers with high-quality and efficient R&D support services to help customers reduce product quality risks.
In 2020, in order to better provide customers with compliant and efficient PCBA services for medical equipment, ABP established a quality management system covering the entire service process of medical products, and passed the on-site audit in November 2020.
ISO 13485:2016 is the standard for a Quality Management System for the design and manufacture of Medical Devices. “ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met the requirements in ISO 13485. The successful passing of ISO13485 means that ABP’s quality management has reached international standards. This is not only an affirmation of ABP’s existing management system, but also an important milestone in the development process.
In the future, ABP Electronics Limited will take the international management level as the basic guarantee, and is committed to providing customers with high-quality and efficient R&D support services to help customers reduce product quality risks.
In 2020, in order to better provide customers with compliant and efficient PCBA services for medical equipment, ABP established a quality management system covering the entire service process of medical products, and passed the on-site audit in November 2020.
ISO 13485:2016 is the standard for a Quality Management System for the design and manufacture of Medical Devices. “ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met the requirements in ISO 13485. The successful passing of ISO13485 means that ABP’s quality management has reached international standards. This is not only an affirmation of ABP’s existing management system, but also an important milestone in the development process.
In the future, ABP Electronics Limited will take the international management level as the basic guarantee, and is committed to providing customers with high-quality and efficient R&D support services to help customers reduce product quality risks.
We are pleased to inform you that we have successfully passed the audit and be certified with ISO 13485:2016.
We are pleased to inform you that we have successfully passed the audit and be certified with ISO 13485:2016.
In 2020, in order to better provide customers with compliant and efficient PCBA services for medical equipment, ABP established a quality management system covering the entire service process of medical products, and passed the on-site audit in November 2020.
ISO 13485:2016 is the standard for a Quality Management System for the design and manufacture of Medical Devices. “ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met the requirements in ISO 13485. The successful passing of ISO13485 means that ABP’s quality management has reached international standards. This is not only an affirmation of ABP’s existing management system, but also an important milestone in the development process.
In the future, ABP Electronics Limited will take the international management level as the basic guarantee, and is committed to providing customers with high-quality and efficient R&D support services to help customers reduce product quality risks.
In 2020, in order to better provide customers with compliant and efficient PCBA services for medical equipment, ABP established a quality management system covering the entire service process of medical products, and passed the on-site audit in November 2020.
ISO 13485:2016 is the standard for a Quality Management System for the design and manufacture of Medical Devices. “ISO 13485 Certified” means an organization has implemented an ISO 13485 Quality Management System and has successfully met the requirements in ISO 13485. The successful passing of ISO13485 means that ABP’s quality management has reached international standards. This is not only an affirmation of ABP’s existing management system, but also an important milestone in the development process.
In the future, ABP Electronics Limited will take the international management level as the basic guarantee, and is committed to providing customers with high-quality and efficient R&D support services to help customers reduce product quality risks.
