# FDA Inspection 789063 - FujiFilm SonoSite, Inc. - July 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/b4e4e21b-ffbc-47af-a5b5-2640c99f50f7
Source feed: FDA_Inspections

> FDA Inspection 789063 for FujiFilm SonoSite, Inc. on July 06, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 789063
- Company Name: FujiFilm SonoSite, Inc.
- Inspection Date: 2012-07-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 789063 - 2012-07-06](https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/cd55f2b9-cf95-4aea-82a9-cf08a2215a56)
- [FDA Inspection 655448 - 2010-04-02](https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/4bf30c6f-d232-4d72-af68-05d16e38d525)
- [FDA Inspection 655448 - 2010-04-02](https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/50ff3568-996a-47f5-841e-f9c323ba6306)

Company: https://www.keypedia.com/companies/fujifilm-sonosite-inc/aec69768-9ce4-44cb-8172-0809e9ee0081

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