Aside from maintaining proper working order for your instruments and devices, it is crucial to consistently calibrate and validate your systems in order to meet compliance standards. Sustaining proper documentation and reports is critical when it comes time for audit reviews. Failure to comply with regulations could result in consequences for your company or facility, such as a Form 483 issued against any observed conditions that may violate the Food Drug and Cosmetic Act.
Mesa Monitoring has services and documentation available to keep your systems working properly and help protect you when it comes to regulatory compliance. We offer on-site services in addition to customized Calibration Certifications. For more information, please contact your Mesa representative.
Please see our Validation website at mesavalidations.com for more information and to find a link for FDA Form 483 warning letters.
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