# FujiFilm SonoSite, Inc. – FDA Inspection, Apr 2, 2010

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/50ff3568-996a-47f5-841e-f9c323ba6306
Source feed: FDA_Inspections

> FDA inspection 655448 of FujiFilm SonoSite, Inc., April 02, 2010. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 655448
- Company Name: FujiFilm SonoSite, Inc.
- Inspection Date: 2010-04-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- FDA Inspection 1041820 - 2017-08-31
- [FDA Inspection 993599 - 2016-10-02](https://www.keypedia.com/records/fda_inspections/fujifilm-sonosite-inc/ac2e28a6-71c2-4516-ae59-6be62132c09c)
- FDA Inspection 789063 - 2012-07-06

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