# Prospera Corporation – FDA Inspection, Oct 20, 2017

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

> FDA inspection 1029410 of Prospera Corporation, October 20, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/quynh-strandberg/9b582ae6-85f9-4163-8ce6-b179c5fd340e)

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

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