# FDA 483 - Monitor Instruments, Inc. - October 10, 2019

Source: https://www.keypedia.com/records/483/monitor-instruments-inc/969d9d9e-0c55-4ef7-ab30-9c0edd7c96ec

> FDA 483 for Monitor Instruments, Inc. on October 10, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Monitor Instruments, Inc.
- Inspection Date: 2019-10-10
- Product Type: device
- Office Name: Atlanta District Office
- Summary: An FDA inspection of Monitor Instruments, Inc. in Hillsborough, NC, conducted on October 9-10, 2019, revealed a significant issue with equipment calibration. The firm failed to adequately establish procedures for routine calibration, inspection, checking, and maintenance of equipment. Specifically, several electronic test instruments were found to have exceeded their assigned 2-year calibration due dates.

## Related Officers

- [Christopher B. May](https://www.keypedia.com/people/christopher-b-may/b2173a59-d37b-41f1-aa39-eefd854722b8)

Company: https://www.keypedia.com/companies/monitor-instruments-inc/9a8d06ca-9cbe-40fa-8fdf-312c1fedf115

Office: https://www.keypedia.com/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7