# FDA Inspection 922290 - Fuji Systems Corporation - March 27, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/fuji-systems-corporation/db3f6a50-6260-4ce6-9230-cc5ed195ddf9
Source feed: FDA_Inspections

> FDA Inspection 922290 for Fuji Systems Corporation on March 27, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 922290
- Company Name: Fuji Systems Corporation
- Inspection Date: 2015-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 922290 - 2015-03-27](https://www.globalkeysolutions.net/records/fda_inspections/fuji-systems-corporation/0c17a8d1-5dd1-4591-a0fe-8d308245158c)
- [FDA Inspection 662115 - 2010-04-29](https://www.globalkeysolutions.net/records/fda_inspections/fuji-systems-corporation/76f74e98-3464-49ce-9e68-01058387fb6a)

Company: https://www.globalkeysolutions.net/companies/fuji-systems-corporation/3c62eb3b-007e-4a7a-9a10-762c10844fb1

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