# FDA Inspection 864939 - Hitachi Aloka Medical, Ltd. - January 24, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/hitachi-aloka-medical-ltd/dfc0d270-8db6-42e2-a994-9f067f984fe4
Source feed: FDA_Inspections

> FDA Inspection 864939 for Hitachi Aloka Medical, Ltd. on January 24, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 864939
- Company Name: Hitachi Aloka Medical, Ltd.
- Inspection Date: 2014-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 864939 - 2014-01-24](https://www.globalkeysolutions.net/records/fda_inspections/hitachi-aloka-medical-ltd/7bd98a7a-28b3-4559-aec5-550e3c508505)
- [FDA Inspection 754077 - 2011-11-16](https://www.globalkeysolutions.net/records/fda_inspections/hitachi-aloka-medical-ltd/9fd698a4-935c-427d-9efc-6373ff90bdd5)

Company: https://www.globalkeysolutions.net/companies/hitachi-aloka-medical-ltd/1a7671ee-c67e-40e1-878f-82ddb36c4251

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