# FDA Inspection 559905 - Fiatlux Imaging - January 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/fiatlux-imaging/a2eef20c-9d28-43a5-a4c9-8ee75d1cd0f5
Source feed: FDA_Inspections

> FDA Inspection 559905 for Fiatlux Imaging on January 22, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559905
- Company Name: Fiatlux Imaging
- Inspection Date: 2009-01-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 700632 - 2010-11-18](https://www.keypedia.com/records/fda_inspections/fiatlux-imaging/e1225db4-a2a1-4e11-a492-ae6fcfa90a17)
- [FDA Inspection 700632 - 2010-11-18](https://www.keypedia.com/records/fda_inspections/fiatlux-imaging/5dd0d46b-ceee-459d-b510-e516088c003d)
- [FDA Inspection 559905 - 2009-01-22](https://www.keypedia.com/records/fda_inspections/fiatlux-imaging/a753eecd-aaf5-41f7-872b-5cb991a19999)

Company: https://www.keypedia.com/companies/fiatlux-imaging/eebcb881-ed6f-403d-84cd-0a5cd74d4471

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