# LD Technology, LLC – FDA Inspection, Jun 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/ld-technology-llc/764e6e00-e06b-4d96-bb40-900366c9bd6a
Source feed: FDA_Inspections

> FDA inspection 670694 of LD Technology, LLC, June 29, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 670694
- Company Name: LD Technology, LLC
- Inspection Date: 2010-06-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1255679 - 2024-11-14
- [FDA Inspection 1190293 - 2022-11-09](https://www.keypedia.com/records/fda_inspections/ld-technology-llc/e4866fcc-d89f-434c-bff5-6312703bc0b9)
- FDA Inspection 1112610 - 2019-12-13
- [FDA Inspection 924934 - 2015-05-05](https://www.keypedia.com/records/fda_inspections/ld-technology-llc/f633be34-5058-40de-a59f-87dafe54bf18)
- FDA Inspection 754378 - 2011-10-27

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
