# FDA Inspection 946034 - Mizuho Corporation Gosen Factory - September 03, 2015

Source: https://www.keypedia.com/records/fda_inspections/mizuho-corporation-gosen-factory/a4d447cd-d5ad-48b2-9faa-09be57a1bfa9
Source feed: FDA_Inspections

> FDA Inspection 946034 for Mizuho Corporation Gosen Factory on September 03, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 946034
- Company Name: Mizuho Corporation Gosen Factory
- Inspection Date: 2015-09-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/mizuho-corporation-gosen-factory/a5d9d895-032f-474d-aef8-893fb8da1e2f

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