# FDA Inspection 803541 - Spes Medica srl - October 04, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/spes-medica-srl/c37417a0-b045-4a0b-9912-91f1685f2f50
Source feed: FDA_Inspections

> FDA Inspection 803541 for Spes Medica srl on October 04, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803541
- Company Name: Spes Medica srl
- Inspection Date: 2012-10-04
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/spes-medica-srl/1665c902-feac-46ab-8a7b-ff3ec58f9d8b

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