# FDA Inspection 964787 - Invatec S.p.A. - February 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/invatec-spa/fdb810dc-cfb0-4237-bc70-23b3eacd4a1b/
Source feed: FDA_Inspections

> FDA Inspection 964787 for Invatec S.p.A. on February 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 964787
- Company Name: Invatec S.p.A.
- Inspection Date: 2016-02-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 964787 - 2016-02-19](https://www.globalkeysolutions.net/api/records/fda_inspections/invatec-spa/6a3c88c2-71f6-4d30-b642-42ef1d5bbed0/)
- [FDA Inspection 876506 - 2014-04-11](https://www.globalkeysolutions.net/api/records/fda_inspections/invatec-spa/aab929f8-7908-4279-af57-10bc14fe3b68/)
- [FDA Inspection 818455 - 2013-02-07](https://www.globalkeysolutions.net/api/records/fda_inspections/invatec-spa/d3e7177d-5f96-43d7-bf9b-df2cdb107363/)

Company: https://www.globalkeysolutions.net/companies/invatec-spa/47dcc3d3-875a-45ba-8d1c-c555f884c562

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