# LDR Medical – FDA Inspection, Apr 7, 2025

Source: https://www.keypedia.com/records/fda_inspections/ldr-medical/50813f61-3990-4d97-b06d-0da66befa121
Source feed: FDA_Inspections

> FDA inspection 1266093 of LDR Medical, April 07, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1266093
- Company Name: LDR Medical
- Inspection Date: 2025-04-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 905792 - 2014-12-04
- [FDA Inspection 600305 - 2009-07-09](https://www.keypedia.com/records/fda_inspections/ldr-medical/c79798fb-9deb-4f11-b6ed-d584b9defd5d)

## Related Officers

- [Investigator](https://www.keypedia.com/people/nadia-r-barreda/ef624359-957a-45e4-89c9-5b5ff215c6aa)

Company: https://www.keypedia.com/companies/ldr-medical/edd56352-8484-418e-9b33-c35631b60092

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