# FDA Inspection 1200950 - FUJIFILM Healthcare Manufacturing Corp. - March 10, 2023

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/0779d496-c79c-4d79-93a3-2dc7de177f3b
Source feed: FDA_Inspections

> FDA Inspection 1200950 for FUJIFILM Healthcare Manufacturing Corp. on March 10, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200950
- Company Name: FUJIFILM Healthcare Manufacturing Corp.
- Inspection Date: 2023-03-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200950 - 2023-03-10](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/66a06d95-9a25-4685-9249-7c660ae2dc0d)
- [FDA Inspection 1200950 - 2023-03-10](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/40995f87-c21b-4712-8b2c-16d5068fb884)
- [FDA Inspection 870122 - 2014-02-19](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/49b5401e-884a-4e37-96a5-d1fc98a2a484)

Company: https://www.keypedia.com/companies/fujifilm-healthcare-manufacturing-corp/e9719a48-f07f-4796-a2a1-fb10779bfb29

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