Compliance and Tracking System

Ximedica is committed to maintaining a fully compliant product development and manufacturing facility. Our records are regularly reviewed and audited by both clients and regulatory bodies.

Ximedica has developed a proprietary database for maintaining compliance related information. This system has passed numerous audits by both the FDA and ISO examiners. It manages everything from initial quotation to product shipments and service life records: including document control, bill of materials management, calibration, corrective and preventative actions, and nonconformance reporting.

Clients can be confident that the information related to their devices is being properly managed and maintained by Ximedica. We are prepared to meet whatever requirements are necessary to keep a client's program properly documented.