# FDA Inspection 1043999 - IGEA SPA - February 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/igea-spa/aa7af2f8-e815-450d-9dda-936690f701d6
Source feed: FDA_Inspections

> FDA Inspection 1043999 for IGEA SPA on February 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043999
- Company Name: IGEA SPA
- Inspection Date: 2018-02-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/igea-spa/4a9e0f9c-8f80-4343-a3dd-8a2461e01275

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