# FDA Inspection 1065344 - Micromed S.p.A. - August 29, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/micromed-spa/5e4fd503-9431-4fc0-a66d-4728455ae8c0
Source feed: FDA_Inspections

> FDA Inspection 1065344 for Micromed S.p.A. on August 29, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065344
- Company Name: Micromed S.p.A.
- Inspection Date: 2018-08-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 915525 - 2015-02-11](https://www.globalkeysolutions.net/records/fda_inspections/micromed-spa/68c75026-7518-488d-a426-340b672ef8ad)
- [FDA Inspection 804734 - 2012-09-19](https://www.globalkeysolutions.net/records/fda_inspections/micromed-spa/fbdfb9d7-ef7d-4413-8717-c4e3c8c65d6f)

Company: https://www.globalkeysolutions.net/companies/micromed-spa/29ce3fb1-fab2-4cad-8598-05feb62d48f9

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