# FDA Inspection 808890 - Fisioline s.r.l. - November 01, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/fisioline-srl/682bd9fb-bf88-4413-ad3e-6f0cda6b5b15
Source feed: FDA_Inspections

> FDA Inspection 808890 for Fisioline s.r.l. on November 01, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808890
- Company Name: Fisioline s.r.l.
- Inspection Date: 2012-11-01
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 808890 - 2012-11-01](https://www.globalkeysolutions.net/records/fda_inspections/fisioline-srl/7f44dd04-a8ad-4ef0-9e96-1cfcab666eaa)

Company: https://www.globalkeysolutions.net/companies/fisioline-srl/3f210e11-1be8-4c6e-bea6-1805c5cad149

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