# FDA Inspection 824384 - Leone S.p.A. - February 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/leone-spa/3d6eff47-eeb0-4d24-9b90-5bd85d3c82d3
Source feed: FDA_Inspections

> FDA Inspection 824384 for Leone S.p.A. on February 21, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824384
- Company Name: Leone S.p.A.
- Inspection Date: 2013-02-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 604471 - 2009-06-11](https://www.keypedia.com/records/fda_inspections/leone-spa/6dac9c9d-fb59-48b4-b4b4-c973033d5b51)

Company: https://www.keypedia.com/companies/leone-spa/4008a0f1-b69e-4cc8-94bd-f9cd62cade04

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