# FDA Inspection 1095860 - FUJIFILM Healthcare Americas Corporation - June 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/482ddb56-56bc-412a-9d42-3e6a54921139
Source feed: FDA_Inspections

> FDA Inspection 1095860 for FUJIFILM Healthcare Americas Corporation on June 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095860
- Company Name: FUJIFILM Healthcare Americas Corporation
- Inspection Date: 2019-06-21
- 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-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