# PRS Medical Technologies Inc. – FDA Inspection, Dec 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/prs-medical-technologies-inc/cb09457c-128e-4840-a134-1ff900b611c5
Source feed: FDA_Inspections

> FDA inspection 1000138 of PRS Medical Technologies Inc., December 19, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000138
- Company Name: PRS Medical Technologies Inc.
- Inspection Date: 2016-12-19
- 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: 4

## Related Officers

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

Company: https://www.keypedia.com/companies/prs-medical-technologies-inc/88bae66e-f381-4e80-b74a-ab1b00255244

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