# Fujifilm Medical Systems USA, Inc. – FDA Inspection, Nov 22, 2013

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-medical-systems-usa-inc/9055fb4b-6ed6-4324-9af3-f0a3f155b4de
Source feed: FDA_Inspections

> FDA inspection 856397 of Fujifilm Medical Systems USA, Inc., November 22, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 856397
- Company Name: Fujifilm Medical Systems USA, Inc.
- Inspection Date: 2013-11-22
- 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: 2

Company: https://www.keypedia.com/companies/fujifilm-medical-systems-usa-inc/c2ee5084-1d12-4fcd-9e63-2ce5cfee291d

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