# FujiFilm Healthcare Americas Corporation – FDA Inspection, Feb 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/d187ec97-a549-498d-a2f9-8b8d1c1c624a
Source feed: FDA_Inspections

> FDA inspection 1000709 of FujiFilm Healthcare Americas Corporation, February 06, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000709
- Company Name: FujiFilm Healthcare Americas Corporation
- Inspection Date: 2017-02-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 824478 - 2013-04-08](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/985457b2-a8be-475d-92a6-5c1450518a85)
- [FDA Inspection 640242 - 2010-02-01](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/dfa20eeb-6f60-4891-9115-0f8229576aac)
- [FDA Inspection 605222 - 2009-08-04](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/e7c6aa0b-6b40-4da6-b692-cd4c13193fa7)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

Company: https://www.keypedia.com/companies/fujifilm-healthcare-americas-corporation/61802929-c43c-4a3a-8773-672bffc28e0c

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