Notice of Completion of ISO 13485 Surveillance Audit
2025.07.07
We are pleased to announce that our Tokyo Headquarters Plant and Chiba Plant underwent the ISO 13485 (Quality Management System for Medical Devices) surveillance audit in June 2025. Following the audit, the certification body has confirmed that our certification remains valid and appropriate for continuation.
We remain committed to the continuous improvement of our quality management system and to delivering even more reliable products and services.
