We leave no stone unturned.
Nothing enters or leaves our facility without rigorous inspection and testing.
Quality is part of the everyday work.
We take our responsibility to customers seriously. Product efficacy and end-user safety are our top priorities.
Our 65,000-square-foot facility has been registered with the FDA since 2004. Our quality management system has been certified under ISO 13485 and ISO 9001 since 2009.
An enduring devotion to quality.
For over 20 years, our team has manufactured high-quality medical devices and chemical products. The expertise we provide is the culmination of decades of experience.
Certified competence.
We regularly update our training and procedures to align with our customers’ needs, applicable FDA requirements, and ISO standards.
Quality documentation
Contact us for current certificates and documentation relevant to your project.
Ask about documentation