# Medfaxx, Inc. – FDA Inspection, Jul 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/medfaxx-inc/cb0fea87-5db8-4d5c-8ec7-735cd205d156
Source feed: FDA_Inspections

> FDA inspection 1095771 of Medfaxx, Inc., July 10, 2019. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095771
- Company Name: Medfaxx, Inc.
- Inspection Date: 2019-07-10
- 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: 5

## Related Documents

- FDA Inspection 975170 - 2016-06-13
- FDA Inspection 805892 - 2012-11-02
- [FDA Inspection 679076 - 2010-09-02](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/3219988d-01ab-49ec-a844-7d2c8158c393)

## Related Officers

- [Investigator](https://www.keypedia.com/people/christopher-b-may/b2173a59-d37b-41f1-aa39-eefd854722b8)
- [Company Rep](https://www.keypedia.com/people/david-e-lowe/1a2492c2-4a81-4486-b3af-37f6b7b5216a)

Company: https://www.keypedia.com/companies/medfaxx-inc/616e39ee-9a45-474d-8de5-d421a9f77d66

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