# FujiFilm Healthcare Americas Corporation – FDA Inspection, Feb 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-healthcare-americas-corporation/dfa20eeb-6f60-4891-9115-0f8229576aac
Source feed: FDA_Inspections

> FDA inspection 640242 of FujiFilm Healthcare Americas Corporation, February 01, 2010. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803, 806 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 640242
- Company Name: FujiFilm Healthcare Americas Corporation
- Inspection Date: 2010-02-01
- 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: 5

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Company: https://www.keypedia.com/companies/fujifilm-healthcare-americas-corporation/61802929-c43c-4a3a-8773-672bffc28e0c

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