# FDA Inspection 590137 - Fujifilm Corporation - June 11, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-corporation/de1a32a7-d65f-4333-a48f-8dd7fd9555e5
Source feed: FDA_Inspections

> FDA Inspection 590137 for Fujifilm Corporation on June 11, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590137
- Company Name: Fujifilm Corporation
- Inspection Date: 2009-06-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/fujifilm-corporation/6310bc48-89ef-4f36-98c9-1e0294a89e06

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