# FUJIFILM MEDWORK GMBH – FDA Inspection, Mar 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-medwork-gmbh/db18885a-bcaa-454e-ac82-d0b181e76b12
Source feed: FDA_Inspections

> FDA inspection 1264887 of FUJIFILM MEDWORK GMBH, March 26, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1264887
- Company Name: FUJIFILM MEDWORK GMBH
- Inspection Date: 2025-03-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Officers

- [Katlin N. Stubbs](https://www.keypedia.com/people/katlin-n-stubbs/27d70db1-a2e9-4254-a721-c6de655f7626)

Company: https://www.keypedia.com/companies/fujifilm-medwork-gmbh/bcc6526e-6ab5-414d-b05b-f93f1940e3ec

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8