Quality System and ISO Certification

Quality System

Medi/Nuclear maintains a quality system under the requirements of the FDA QSR, 21 CFR Parts 820, Medical Devices; Current Good Manufacturing Practice (CGMP) and Medi/Nuclear’s quality system has been certified in accordance with EN ISO 13485 by TUV Rheinland of North American, Inc. under CMDCAS for Health Canada license.

Quality Policy

“Working together and Quality – it’s what we do”

Medi/Nuclear Corporation, Inc. manufactures and distribute quality medical device products and services that:

• Meets or exceed our customer’s needs and expectation at competitive prices
• Complies with applicable standards and regulations
• Continually improve our products, processes and quality system
• Are driven by our quality objectives
• And our team members are empowered to delight our customers