# FUJIFILM Healthcare Americas Corporation – FDA Inspection, Oct 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/945c2309-d1e2-4202-b58d-2bbd97355afa
Source feed: FDA_Inspections

> FDA inspection 991423 of FUJIFILM Healthcare Americas Corporation, October 31, 2016. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991423
- Company Name: FUJIFILM Healthcare Americas Corporation
- Inspection Date: 2016-10-31
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1095860 - 2019-06-21](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/482ddb56-56bc-412a-9d42-3e6a54921139)
- [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 919044 - 2015-02-19
- FDA Inspection 810738 - 2012-12-12

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)

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