# Medifocus, Inc. – FDA Inspection, Dec 3, 2015

Source: https://www.keypedia.com/records/fda_inspections/medifocus-inc/722bba86-5329-4142-9eaf-ddcc16f6303d
Source feed: FDA_Inspections

> FDA inspection 953902 of Medifocus, Inc., December 03, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953902
- Company Name: Medifocus, Inc.
- Inspection Date: 2015-12-03
- 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: 3

## Related Documents

- [FDA Inspection 1080032 - 2019-02-21](https://www.keypedia.com/records/fda_inspections/medifocus-inc/ebdc5e9b-22f8-4c23-b75c-96e6743590f0)
- FDA Inspection 828779 - 2013-04-26

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