FDA Inspection
Ellex iScience, Inc.Ellex iScience, Inc. – FDA Inspection, Aug 16, 2010
Record Details
This FDA Inspection record concerns Ellex iScience, Inc., with an inspection on August 16, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ellex iScience, Inc.
- Inspection Date
- August 16, 2010
- Product Type
- Devices
View Company Profile
ID · 8c99dafb-aff8-4003-a00c-7af15de9b62b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 675218
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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 | |
| September 8, 2017 | 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 |
Other documents for Ellex iScience, Inc.
- FDA Inspection 1094990 - 2018-12-07
- FDA Inspection 1094978 - 2018-06-12
- FDA Inspection 1034615 - 2017-09-08
- FDA Inspection 931524 - 2015-06-25
- FDA Inspection 823616 - 2013-03-27
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