# FUJIFILM Healthcare Manufacturing Corporation Sano Office – FDA Inspection, Jan 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 of FUJIFILM Healthcare Manufacturing Corporation Sano Office, January 27, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## 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)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

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