# FDA 483 - Mid South Precision, Inc. - May 12, 2025

Source: https://www.keypedia.com/records/483/mid-south-precision-inc/aebeda3d-67de-4c12-80d7-832e7bf5bf63

> FDA 483 for Mid South Precision, Inc. on May 12, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Mid South Precision, Inc.
- Inspection Date: 2025-05-12
- Product Type: device
- Office Name: New Orleans District Office
- Summary: An FDA inspection of Mid South Precision, Inc. in Murfreesboro, TN, a manufacturer of Class I and Class II medical devices, revealed significant quality system deficiencies. The firm received three observations, two of which were repeat observations from previous inspections, highlighting failures in process validation, corrective and preventive actions, and environmental controls for raw materials. These issues indicate a lack of adequate control over manufacturing processes and product quality.

## Related Documents

- [483 - 2021-10-25](https://www.keypedia.com/records/483/mid-south-precision-inc/ade5e7e9-e611-4971-9573-d59f34d2f03a)

## Related Officers

- [Jamie P. Webb](https://www.keypedia.com/people/jamie-p-webb/9e052469-54f7-4d56-b977-27babbdac09b)

Company: https://www.keypedia.com/companies/mid-south-precision-inc/7ed596d0-66f8-47e5-a004-8174d047c7f0

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea