FDA Inspection
FujiFilm SonoSite, Inc.FujiFilm SonoSite, Inc. – FDA Inspection, Jun 21, 2019
Record Details
This FDA Inspection record concerns FujiFilm SonoSite, Inc., with an inspection on June 21, 2019, issued by the Seattle District Office, covering medical devices & rad health.
- Company
- FujiFilm SonoSite, Inc.
- Inspection Date
- June 21, 2019
- Product Type
- Medical Devices & Rad Health
- Office
- Seattle District Office
View Company Profile
ID · 0148234a-7038-49df-9252-0b8ff0a684cd
Inspection Facts
- Inspection number
- 1141444
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of FujiFilm SonoSite, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 31, 2017 | Not classified | Seattle District Office | |
| October 2, 2016 | Not classified | Seattle District Office | |
| July 6, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 2, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for FujiFilm SonoSite, Inc.
- FDA Inspection 1041820 - 2017-08-31
- FDA Inspection 993599 - 2016-10-02
- FDA Inspection 789063 - 2012-07-06
- FDA Inspection 655448 - 2010-04-02
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