# FDA Inspection 600305 - LDR Medical - July 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/ldr-medical/c79798fb-9deb-4f11-b6ed-d584b9defd5d
Source feed: FDA_Inspections

> FDA Inspection 600305 for LDR Medical on July 09, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 600305
- Company Name: LDR Medical
- Inspection Date: 2009-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1266093 - 2025-04-07](https://www.keypedia.com/records/fda_inspections/ldr-medical/0c558c0f-f0e8-47a1-90a3-71246093b38e)
- [FDA Inspection 1266093 - 2025-04-07](https://www.keypedia.com/records/fda_inspections/ldr-medical/50813f61-3990-4d97-b06d-0da66befa121)
- [FDA Inspection 905792 - 2014-12-04](https://www.keypedia.com/records/fda_inspections/ldr-medical/592366b1-860f-4108-b185-c997536a9f5a)
- [FDA Inspection 600305 - 2009-07-09](https://www.keypedia.com/records/fda_inspections/ldr-medical/80cc624a-4fd1-42a5-a34c-8ad64632bf76)

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