# FDA Inspection 559923 - Lordex, Inc - January 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/lordex-inc/1781378f-394b-42c0-a15b-f293230a8d44
Source feed: FDA_Inspections

> FDA Inspection 559923 for Lordex, Inc on January 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559923
- Company Name: Lordex, Inc
- Inspection Date: 2009-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lordex-inc/e7942de0-8d0c-4dae-b60a-7d9e631f3a96

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