# FDA Inspection 1029410 - Prospera Corporation - October 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/prospera-corporation/522c58d5-25ac-40e0-a5ce-985a1300f596
Source feed: FDA_Inspections

> FDA Inspection 1029410 for Prospera Corporation on October 20, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029410
- Company Name: Prospera Corporation
- Inspection Date: 2017-10-20
- 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 1029410 - 2017-10-20](https://www.globalkeysolutions.net/records/fda_inspections/prospera-corporation/027b806d-da6e-465a-8287-a4d0f5b7f7cd)

Company: https://www.globalkeysolutions.net/companies/prospera-corporation/7f5ef236-90f5-48ca-a83d-4f23bc9dc3ab

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