Our commitment to quality is built around our ISO 13485 certification and our dedication to serving the medical device industry. We received our initial registration of device establishment from the FDA in 1988, officially registered in 1989 and continue to comply with all regulations and requirements. Our quality practices and procedures are based on lean manufacturing principles and go beyond industry standards to provide our customers with unparalleled accuracy and unmatched precision. Our dedication to quality serves as the foundation of the company as we strive for excellence in every part we manufacture.
Our commitment to serving the medical device industry combined with over thirty years of contract manufacturing experience allows us to effectively manufacture to our customer’s specifications. The result being added value for our customers through great quality, delivery and service.
Our Quality Policy
Anjon Holdings is committed to meeting customer and regulatory requirements by maintaining an effective quality management system.
We produce both product for sale under our own design control, and both finished an unfinished medical devices as a contract manufacture.
We keep in mind the lives of the patients that we help and manage product risk with the patient in mind as if a member of our own families.
As a commitment to quality, we ensure compliance with applicable medical device regulations.
We strive to continually improve ourselves and to ensure we provide reliable and cost-effective solutions to our customers’ needs.