Company
United StatesFujiFilm SonoSite, Inc., Bothell, WA – FDA Inspections
Inspection records and compliance data for FujiFilm SonoSite, Inc. in Bothell, Washington. 5 FDA inspections on record, 2 Form 483s, last inspected June 21, 2019.
Company Profile
This profile covers FujiFilm SonoSite, Inc. based in Bothell, Washington, United States.
FDA Inspection History
- FDA inspections
- 5
- OAI
- 0
- VAI
- 0
- NAI
- 2
- Unclassified
- 3
- Form 483s
- 2
- Warning letters
- 0
First inspected April 2, 2010. Last inspected June 21, 2019.
FDA inspections (5)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| June 21, 2019 | Not classified | Medical Devices & Rad Health | 1141444 |
| August 31, 2017 | Not classified | Medical Devices & Rad Health | 1041820 |
| October 2, 2016 | Not classified | Medical Devices & Rad Health | 993599 |
| July 6, 2012 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 789063 |
| April 2, 2010 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 655448 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
FujiFilm SonoSite, Inc.
FEI Number
3002087856
Address
21919 30th Dr Se, Bothell, Washington 98021, United States
Country
United States
ID: aec69768-9ce4-44cb-8172-0809e9ee0081