# FDA 483 - LD Technology, LLC - December 13, 2019

Source: https://www.globalkeysolutions.net/records/483/ld-technology-llc/8e4c316d-5da7-4023-9959-3aa695ff39ad

> FDA 483 for LD Technology, LLC on December 13, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: LD Technology, LLC
- Inspection Date: 2019-12-13
- Product Type: device
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: ET Technology, LLC in Miami, FL, a specification developer, was cited with three observations during an FDA inspection. The firm failed to adequately establish and implement procedures for complaint handling, corrective and preventive actions (CAPA), and document control. These issues indicate significant deficiencies in their quality system.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/karen-m-rodriguez/fcef1f49-583d-45ab-80e2-4c34793fd722)

Company: https://www.globalkeysolutions.net/companies/ld-technology-llc/b4571124-5825-41df-97b1-528466a31e47

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