# FDA Inspection 1198537 - Phoenix Deventures - February 15, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/phoenix-deventures/42ae32a4-1f45-43e6-ad17-e74aef307f9f
Source feed: FDA_Inspections

> FDA Inspection 1198537 for Phoenix Deventures on February 15, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1198537
- Company Name: Phoenix Deventures
- Inspection Date: 2023-02-15
- 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 1014716 - 2017-05-04](https://www.globalkeysolutions.net/records/fda_inspections/phoenix-deventures/ffb2024f-fff5-4873-b923-a3e6f9b98e73)
- [FDA Inspection 857368 - 2013-12-06](https://www.globalkeysolutions.net/records/fda_inspections/phoenix-deventures/797c1083-328b-497c-aa75-378d71874970)
- [FDA Inspection 857368 - 2013-12-06](https://www.globalkeysolutions.net/records/fda_inspections/phoenix-deventures/ef9b1ab3-a760-4197-8855-057c70f04073)

Company: https://www.globalkeysolutions.net/companies/phoenix-deventures/660e347c-a07b-4d8b-9569-7132bfa22e37

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