# FDA Inspection 952050 - Ionisos - December 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/ionisos/60b32934-c677-419e-a8e4-97e1ed978236
Source feed: FDA_Inspections

> FDA Inspection 952050 for Ionisos on December 10, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 952050
- Company Name: Ionisos
- Inspection Date: 2015-12-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ionisos/53ec7d88-e3fe-4be5-92cd-6befc0cc0864

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