# MedImage, Inc. – FDA Inspection, Nov 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/medimage-inc/e22bc5c1-c288-4e14-bbb2-6267b64f1855
Source feed: FDA_Inspections

> FDA inspection 1030952 of MedImage, Inc., November 02, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1030952
- Company Name: MedImage, Inc.
- Inspection Date: 2017-11-02
- 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 1256107 - 2024-11-14
- FDA Inspection 907723 - 2014-12-22
- [FDA Inspection 828568 - 2013-04-23](https://www.keypedia.com/records/fda_inspections/medimage-inc/37110d40-270a-482a-b093-e53211d1502e)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/medimage-inc/71c52a29-6062-42b0-8406-4092eec1cc80

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