# iCAD, Inc. – FDA Inspection, Jul 2, 2015

Source: https://www.keypedia.com/records/fda_inspections/icad-inc/ac5a88a6-2f7a-472f-a5b9-188427706ae6
Source feed: FDA_Inspections

> FDA inspection 935201 of iCAD, Inc., July 02, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935201
- Company Name: iCAD, Inc.
- Inspection Date: 2015-07-02
- 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: 1

## Related Documents

- FDA Inspection 1146145 - 2021-05-25
- FDA Inspection 830427 - 2013-05-07
- FDA Inspection 721926 - 2011-04-19
- FDA Inspection 571386 - 2009-03-18

Company: https://www.keypedia.com/companies/icad-inc/7726a6c9-7e7f-4aad-a45a-141da09fc401

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