# Eurospital S.P.A. – FDA Inspection, Feb 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/eurospital-spa/eb1b0226-f691-4624-a74e-3763cc3fe457
Source feed: FDA_Inspections

> FDA inspection 770910 of Eurospital S.P.A., February 23, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 770910
- Company Name: Eurospital S.P.A.
- Inspection Date: 2012-02-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1028360 - 2017-07-07](https://www.keypedia.com/records/fda_inspections/eurospital-spa/d4e1c767-4cb8-46d9-b241-6385d6f92c91)

Company: https://www.keypedia.com/companies/eurospital-spa/d3385294-0346-4aa6-bd97-49e21dd8296c

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