# LDR Medical – FDA Inspection, Jul 9, 2009

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

> FDA inspection 600305 of LDR Medical, July 09, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations 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: 600305
- Company Name: LDR Medical
- Inspection Date: 2009-07-09
- 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: 3

## Related Documents

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- FDA Inspection 905792 - 2014-12-04

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