# Phoenix Diagnostics, Inc. – FDA Inspection, Aug 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/phoenix-diagnostics-inc/fd34080b-275f-46d4-9da2-a471a13af3b6
Source feed: FDA_Inspections

> FDA inspection 1022108 of Phoenix Diagnostics, Inc., August 18, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022108
- Company Name: Phoenix Diagnostics, Inc.
- Inspection Date: 2017-08-18
- 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: 6

## Related Documents

- FDA Inspection 1164713 - 2022-03-17
- [FDA Inspection 792557 - 2012-07-26](https://www.keypedia.com/records/fda_inspections/phoenix-diagnostics-inc/dacd52aa-c5f5-4638-bb09-78dadfdc6e09)
- FDA Inspection 602295 - 2009-08-06

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)

Company: https://www.keypedia.com/companies/phoenix-diagnostics-inc/e6758401-487c-47a5-8942-ac7f5e87b05a

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