# FDA Inspection 1007160 - Fuji Dynamics Limited - March 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/fuji-dynamics-limited/9fd6a16c-d3fa-4078-bf72-4937ce11c910
Source feed: FDA_Inspections

> FDA Inspection 1007160 for Fuji Dynamics Limited on March 09, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007160
- Company Name: Fuji Dynamics Limited
- Inspection Date: 2017-03-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110342 - 2019-10-24](https://www.keypedia.com/records/fda_inspections/fuji-dynamics-limited/d9d5a80d-5ca8-4264-a0af-02753236d548)
- [FDA Inspection 1007160 - 2017-03-09](https://www.keypedia.com/records/fda_inspections/fuji-dynamics-limited/2f563711-bf59-4409-8ab1-b29df2d4d313)

Company: https://www.keypedia.com/companies/fuji-dynamics-limited/d26a8e37-2ed6-4a70-b2c6-c53e5422fa20

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