# FDA Inspection 1037713 - FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa - December 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-corporation-medical-systems-research-development-center-kashiwa/a049320d-0967-4b53-a720-ebe6c8de83e8
Source feed: FDA_Inspections

> FDA Inspection 1037713 for FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa on December 21, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037713
- Company Name: FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa
- Inspection Date: 2017-12-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/fujifilm-corporation-medical-systems-research-development-center-kashiwa/3b1ccab4-807f-4991-88c5-b2073133847d

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