# FDA 483 - Princeton Medical Group Inc - November 21, 2023

Source: https://www.globalkeysolutions.net/records/483/princeton-medical-group-inc/94af3c43-c341-43b6-9e31-5005a42d009b

> FDA 483 for Princeton Medical Group Inc on November 21, 2023. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Princeton Medical Group Inc
- Inspection Date: 2023-11-21
- Product Type: device
- Office Name: New Orleans District Office
- Summary: Princeton Medical Group Inc, a medical device manufacturer in Franklin, TN, was cited for two significant observations during an FDA inspection. The firm failed to ensure its Class I and Class II medical devices were directly marked with Unique Device Identifiers (UDI) and did not submit required UDI information to the FDA's GUDID. Additionally, the company lacked documented procedures for handling complaints and could not provide complaint files for review.

## Related Officers

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

Company: https://www.globalkeysolutions.net/companies/princeton-medical-group-inc/18925466-bb3f-4d84-8412-631afdc3b5d6

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