# FDA Inspection 605222 - FujiFilm Healthcare Americas Corporation - August 04, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-healthcare-americas-corporation/3cb08966-806c-4fb7-ac66-57d29b47f68c
Source feed: FDA_Inspections

> FDA Inspection 605222 for FujiFilm Healthcare Americas Corporation on August 04, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 605222
- Company Name: FujiFilm Healthcare Americas Corporation
- Inspection Date: 2009-08-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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