# Ellex iScience, Inc. – FDA Inspection, Aug 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/ellex-iscience-inc/8c99dafb-aff8-4003-a00c-7af15de9b62b
Source feed: FDA_Inspections

> FDA inspection 675218 of Ellex iScience, Inc., August 16, 2010. Classification: Voluntary Action Indicated (VAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675218
- Company Name: Ellex iScience, Inc.
- Inspection Date: 2010-08-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: 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 1094978 - 2018-06-12
- [FDA Inspection 1034615 - 2017-09-08](https://www.keypedia.com/records/fda_inspections/ellex-iscience-inc/a69f6668-298b-4e14-9055-9acad418d88b)
- [FDA Inspection 931524 - 2015-06-25](https://www.keypedia.com/records/fda_inspections/ellex-iscience-inc/99264e56-0e9a-4e4a-893b-acd8293893fa)
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Company: https://www.keypedia.com/companies/ellex-iscience-inc/6cfbafeb-cb97-42d7-b825-94e3a63915fb

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
