# Artsana S.p.A. – FDA Inspection, Jul 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/artsana-spa/c2d380dc-6b1f-45f8-97f5-6e917e4a6f42
Source feed: FDA_Inspections

> FDA inspection 1020927 of Artsana S.p.A., July 20, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020927
- Company Name: Artsana S.p.A.
- Inspection Date: 2017-07-20
- 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: 0

## Related Documents

- FDA Inspection 834446 - 2013-05-09
- [FDA Inspection 717756 - 2011-01-27](https://www.keypedia.com/records/fda_inspections/artsana-spa/d453cdde-90d0-4fa2-b43c-a3603fcf211b)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/artsana-spa/2bb6d806-2a76-4eae-b285-313b572ea6af

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