# FDA Inspection 975171 - Fujifilm Healthcare Americas Corporation - May 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/c6d8e9c3-4dfa-4f89-bbd0-31bff3c6a0fc
Source feed: FDA_Inspections

> FDA Inspection 975171 for Fujifilm Healthcare Americas Corporation on May 02, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975171
- Company Name: Fujifilm Healthcare Americas Corporation
- Inspection Date: 2016-05-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 975171 - 2016-05-02](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/5c451196-43a7-4bde-9aa7-212c7de342b8)

Company: https://www.keypedia.com/companies/fujifilm-healthcare-americas-corporation/4e56f053-0b21-445f-aa9a-459e85d732d7

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