# FDA Inspection 1000709 - FujiFilm Healthcare Americas Corporation - February 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/61c0fad1-418a-427e-8953-d1bf8419ed2e
Source feed: FDA_Inspections

> FDA Inspection 1000709 for FujiFilm Healthcare Americas Corporation on February 06, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1000709
- Company Name: FujiFilm Healthcare Americas Corporation
- Inspection Date: 2017-02-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1000709 - 2017-02-06](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/d187ec97-a549-498d-a2f9-8b8d1c1c624a)
- [FDA Inspection 824478 - 2013-04-08](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/946fd00f-da00-43d4-895b-dacc80a01442)
- [FDA Inspection 824478 - 2013-04-08](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/985457b2-a8be-475d-92a6-5c1450518a85)
- [FDA Inspection 640242 - 2010-02-01](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/dfa20eeb-6f60-4891-9115-0f8229576aac)
- [FDA Inspection 640242 - 2010-02-01](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/aff1b226-63a9-425e-87a5-8cf1168d9af6)

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

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