FDA Inspection
Ellex iScience, Inc.Ellex iScience, Inc. – FDA Inspection, Sep 8, 2017
Record Details
This FDA Inspection record concerns Ellex iScience, Inc., with an inspection on September 8, 2017, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Ellex iScience, Inc.
- Inspection Date
- September 8, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · a69f6668-298b-4e14-9055-9acad418d88b
Inspection Facts
- Inspection number
- 1034615
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Ellex iScience, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 7, 2018 | Not classified | San Francisco District Office | |
| June 12, 2018 | Not classified | San Francisco District Office | |
| June 25, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 27, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 16, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ellex iScience, Inc.
- FDA Inspection 1094990 - 2018-12-07
- FDA Inspection 1094978 - 2018-06-12
- FDA Inspection 931524 - 2015-06-25
- FDA Inspection 823616 - 2013-03-27
- FDA Inspection 675218 - 2010-08-16
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