# FDA 483 - Maguire Enterprises, Inc. - June 28, 2023

Source: https://www.keypedia.com/records/483/maguire-enterprises-inc/dd80d4df-b1c0-4d88-818d-81e3d6fd5a49

> FDA 483 for Maguire Enterprises, Inc. on June 28, 2023. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Maguire Enterprises, Inc.
- Inspection Date: 2023-06-28
- Product Type: device
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: Maguire Enterprises, Inc., a medical device manufacturer in Sunrise, FL, was inspected by the FDA from June 26-28, 2023. The inspection revealed a significant issue regarding the labeling of their medical devices. Specifically, the firm's interconnect cables lacked the required unique device identifiers (UDI) on labels and packages.

## Related Officers

- [Dianiris C. Ayala](https://www.keypedia.com/people/dianiris-c-ayala/ba6c5538-201b-4c9a-8f23-e160db6868e6)

Company: https://www.keypedia.com/companies/maguire-enterprises-inc/5c816d6f-2854-4e4d-9c8e-77ab8d4f2c53

Office: https://www.keypedia.com/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6