# FDA Inspection 968511 - Mizuho OSI - February 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/mizuho-osi/b7741585-7fbb-47e6-a897-5dbfb47ba0f7
Source feed: FDA_Inspections

> FDA Inspection 968511 for Mizuho OSI on February 25, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 968511
- Company Name: Mizuho OSI
- Inspection Date: 2016-02-25
- Classification: No Action Indicated (NAI)
- 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/mizuho-osi/adece774-aa31-473f-9e7f-3db559ad73e2

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