# FDA Inspection 1197046 - FUJIFILM Healthcare Manufacturing Corporation Sano Office - January 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-sano-office/126169c2-6376-4023-b1af-c3fff3269bd2
Source feed: FDA_Inspections

> FDA Inspection 1197046 for FUJIFILM Healthcare Manufacturing Corporation Sano Office on January 27, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197046
- Company Name: FUJIFILM Healthcare Manufacturing Corporation Sano Office
- Inspection Date: 2023-01-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1114409 - 2019-09-10](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-sano-office/0f1da8a6-8b19-4bb6-a131-2a5d5394f215)
- [FDA Inspection 928459 - 2015-04-22](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-sano-office/62d8dce0-5a21-4d70-9502-c2d372084921)
- [FDA Inspection 928459 - 2015-04-22](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corporation-sano-office/85b430d9-576e-4484-8ca5-7dc83de5283a)

Company: https://www.keypedia.com/companies/fujifilm-healthcare-manufacturing-corporation-sano-office/6977e0cf-8f74-4413-93e6-dbb6fa474b82

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