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Banister Tool Quality Policy:

Quality Through Commitment

Banister Tool is committed, by demonstrated performance, to the pursuit of excellence in achieving total quality in all our endeavors.

As a company engaged in producing non-active medical devices (primarily medical instruments, implants, and medical apparatuses), we were awarded an ISO 13485:2003 certification in February of 2005 and are committed to its principles, along with Current Good Manufacturing Practices (CGMP), and all statutory and regulatory requirements. We are registered with both the Federal Food and Drug Administration (FDA) and the Texas Department of State Health Services, and are in good standing by audit confirmation. As a contract manufacturer, we are committed to continually improve our processes, and remain focused on our quality objectives.

Quality Through Planning

We stay abreast of international quality regulations and standards, and work in conjunction with our customers to recognize and resolve mutual quality issues. Together, we embrace new ideas, new concepts, and innovations to improve our sovereignty and secure our future.

Quality Through Sharing

We share our technology, manufacturing expertise, our ever-expanding processing capability and capacity with our customers. Thereby, together we meet the challenges of today’s constantly changing business, and secure our share of tomorrow’s marketplace.