# FDA Inspection 1119726 - Mizuho America, Inc. - December 17, 2019

Source: https://www.keypedia.com/records/fda_inspections/mizuho-america-inc/5bd9c2af-cb5c-4c3d-813a-007280ca8803
Source feed: FDA_Inspections

> FDA Inspection 1119726 for Mizuho America, Inc. on December 17, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1119726
- Company Name: Mizuho America, Inc.
- Inspection Date: 2019-12-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1119726 - 2019-12-17](https://www.keypedia.com/records/fda_inspections/mizuho-america-inc/b77399be-ad1e-4567-a04b-5f0c28348a75)

Company: https://www.keypedia.com/companies/mizuho-america-inc/01971116-75c3-4337-89fa-f2a735f62fa1

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