Our modern clean room production facility conforms to the operational requirements of international cleanroom standards. Good Manufacturing Practice (G.M.P) compliance is at the heart of our manufacturing and logistics philosophies.
Extensive product evaluation procedures aim to guarantee confidence in our products and customer satisfaction.We only select suppliers and sub-contractors who meet our stringent purchasing and quality requirements.
Takumi Precision Enfineering is committed to the principles of Total Quality Management, with an integrated Quality Management System which is compliant to the requirements of recognised International Standards and which is continually developed, audited and reviewed.
All products are in compliance with the European Medical Device Directive 93/42/EEC for CE-Marking.
All our products are monitored throughout all stages of development, procurement and manufacture to ensure that conformance to specification is achieved.
Takumi Precision Engineering maintains a comprehensive quality assurance and quality control program. Our quality systems are based upon and in compliance with International Organization for Standardization (ISO) requirements, and where applicable, United States Food and Drug Administration (FDA) regulations.