# Fujifilm Corporation – FDA Inspection, Sep 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-corporation/e7a18e04-1b71-438f-8c2b-3e452a37951b
Source feed: FDA_Inspections

> FDA inspection 1219107 of Fujifilm Corporation, September 22, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1219107
- Company Name: Fujifilm Corporation
- Inspection Date: 2023-09-22
- 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: 6

## Related Documents

- [FDA Inspection 1115949 - 2019-09-30](https://www.keypedia.com/records/fda_inspections/fujifilm-corporation/ec2e2746-01cc-4a9b-b37c-9348ea3b34ba)
- [FDA Inspection 1061550 - 2018-07-13](https://www.keypedia.com/records/fda_inspections/fujifilm-corporation/be6658c6-428b-418e-920c-9931b20a086b)
- FDA Inspection 995868 - 2016-12-08
- FDA Inspection 837192 - 2013-04-25
- FDA Inspection 590137 - 2009-06-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/fujifilm-corporation/6310bc48-89ef-4f36-98c9-1e0294a89e06

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