# FUJIFILM Healthcare Manufacturing Corp. – FDA Inspection, Mar 10, 2023

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/66a06d95-9a25-4685-9249-7c660ae2dc0d
Source feed: FDA_Inspections

> FDA inspection 1200950 of FUJIFILM Healthcare Manufacturing Corp., March 10, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1200950
- Company Name: FUJIFILM Healthcare Manufacturing Corp.
- Inspection Date: 2023-03-10
- 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: 0

## Related Documents

- [FDA Inspection 996016 - 2016-12-14](https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-manufacturing-corp/ee638b84-0917-47da-b6f8-4cd6e8290052)
- FDA Inspection 870122 - 2014-02-19

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

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