# FDA Inspection 907150 - IMS GIOTTO S.p.A. - December 04, 2014

Source: https://www.keypedia.com/records/fda_inspections/ims-giotto-spa/8a50a8a7-32f4-4fd6-8a21-3ebba01ec272
Source feed: FDA_Inspections

> FDA Inspection 907150 for IMS GIOTTO S.p.A. on December 04, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907150
- Company Name: IMS GIOTTO S.p.A.
- Inspection Date: 2014-12-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 907150 - 2014-12-04](https://www.keypedia.com/records/fda_inspections/ims-giotto-spa/d2fce7db-3475-40f8-adfe-241edbaffed9)
- [FDA Inspection 859900 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/ims-giotto-spa/1f241d98-59bd-467a-9aec-0e0e826b0c4a)

Company: https://www.keypedia.com/companies/ims-giotto-spa/c9669b6d-c8a4-4656-b49b-46401a92ce64

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