# FDA Inspection 1095771 - Medfaxx, Inc. - July 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/medfaxx-inc/6dd46de9-105d-434b-b11f-10ad5caffcb9
Source feed: FDA_Inspections

> FDA Inspection 1095771 for Medfaxx, Inc. on July 10, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1095771 - 2019-07-10](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/cb0fea87-5db8-4d5c-8ec7-735cd205d156)
- [FDA Inspection 975170 - 2016-06-13](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/b391eb3b-8811-4e6d-a087-292e5224ed5d)
- [FDA Inspection 975170 - 2016-06-13](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/bc392f49-d96a-4feb-861b-c712afef1182)
- [FDA Inspection 805892 - 2012-11-02](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/2d109a4e-504e-46ff-8a97-d47223182981)
- [FDA Inspection 805892 - 2012-11-02](https://www.keypedia.com/records/fda_inspections/medfaxx-inc/e6bf872a-9688-4967-a68e-a2edbf8a03ab)

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