# FUJIFILM Healthcare Americas Corporation – FDA Inspection, Jun 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 of FUJIFILM Healthcare Americas Corporation, June 21, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1095860
- Company Name: FUJIFILM Healthcare Americas Corporation
- Inspection Date: 2019-06-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1046796 - 2018-03-29](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/dd580004-117e-4a2d-9e7a-5b39653ec7f3)
- FDA Inspection 994698 - 2016-11-10
- [FDA Inspection 991423 - 2016-10-31](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/945c2309-d1e2-4202-b58d-2bbd97355afa)
- FDA Inspection 919044 - 2015-02-19
- FDA Inspection 810738 - 2012-12-12

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

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