# Microstim Technology, Inc. – FDA Inspection, Nov 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/microstim-technology-inc/fc962165-4523-4803-919e-725a3d52f4d9
Source feed: FDA_Inspections

> FDA inspection 997044 of Microstim Technology, Inc., November 18, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997044
- Company Name: Microstim Technology, Inc.
- Inspection Date: 2016-11-18
- 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: 4

## Related Documents

- [FDA Inspection 791510 - 2012-07-16](https://www.keypedia.com/records/fda_inspections/microstim-technology-inc/c4e057d0-6973-4eb2-8876-492d68265bee)
- FDA Inspection 559883 - 2009-02-03

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/microstim-technology-inc/6bf1cb79-390f-489d-a40d-57cd03d78961

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