# Medifocus, Inc. – FDA Inspection, Feb 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/medifocus-inc/ebdc5e9b-22f8-4c23-b75c-96e6743590f0
Source feed: FDA_Inspections

> FDA inspection 1080032 of Medifocus, Inc., February 21, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080032
- Company Name: Medifocus, Inc.
- Inspection Date: 2019-02-21
- 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 953902 - 2015-12-03](https://www.keypedia.com/records/fda_inspections/medifocus-inc/722bba86-5329-4142-9eaf-ddcc16f6303d)
- FDA Inspection 828779 - 2013-04-26

## Related Officers

- [Company Rep](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)

Company: https://www.keypedia.com/companies/medifocus-inc/38d20abc-d043-443a-9e2a-2459b0da9b28

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