# FDA Inspection 795315 - Prowess, Inc. - July 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/prowess-inc/08c2d9e5-4b02-4509-b6d6-62e12b269560
Source feed: FDA_Inspections

> FDA Inspection 795315 for Prowess, Inc. on July 17, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 795315
- Company Name: Prowess, Inc.
- Inspection Date: 2012-07-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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