# FDA Inspection 919044 - FUJIFILM Healthcare Americas Corporation - February 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/408396cc-ff6d-4f85-bc14-ed98817e7a90
Source feed: FDA_Inspections

> FDA Inspection 919044 for FUJIFILM Healthcare Americas Corporation on February 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919044
- Company Name: FUJIFILM Healthcare Americas Corporation
- Inspection Date: 2015-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/fujifilm-healthcare-americas-corporation/2125ef05-abe1-4bb0-953b-31cb8254e1e8

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