# FDA Inspection 1157620 - Prowess, Inc. - November 10, 2021

Source: https://www.globalkeysolutions.net/records/fda_inspections/prowess-inc/fdee814a-63bd-4aaa-b702-9251253e1b08/
Source feed: FDA_Inspections

> FDA Inspection 1157620 for Prowess, Inc. on November 10, 2021. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1157620
- Company Name: Prowess, Inc.
- Inspection Date: 2021-11-10
- 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 795315 - 2012-07-17](https://www.globalkeysolutions.net/api/records/fda_inspections/prowess-inc/9637625b-c622-403b-a8da-6609d1b8058e/)
- [FDA Inspection 795315 - 2012-07-17](https://www.globalkeysolutions.net/api/records/fda_inspections/prowess-inc/08c2d9e5-4b02-4509-b6d6-62e12b269560/)
- [FDA Inspection 675484 - 2010-08-11](https://www.globalkeysolutions.net/api/records/fda_inspections/prowess-inc/a323c0c7-0f02-4d5a-899f-aaeb959f24e3/)
- [FDA Inspection 675484 - 2010-08-11](https://www.globalkeysolutions.net/api/records/fda_inspections/prowess-inc/d90317e5-4149-4f73-b913-3466a0aefc10/)

Company: https://www.globalkeysolutions.net/companies/prowess-inc/6a3b23eb-1386-4b3e-a53e-38848fb05418

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