# Mizuho OSI – FDA Inspection, Sep 11, 2012

Source: https://www.keypedia.com/records/fda_inspections/mizuho-osi/c72d4157-e362-48b9-930e-6b94db00e0ce
Source feed: FDA_Inspections

> FDA inspection 798286 of Mizuho OSI, September 11, 2012. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 798286
- Company Name: Mizuho OSI
- Inspection Date: 2012-09-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 968511 - 2016-02-25
- FDA Inspection 850919 - 2013-09-25
- FDA Inspection 661263 - 2010-06-02

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