# FDA Inspection 1000138 - PRS Medical Technologies Inc. - December 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/prs-medical-technologies-inc/81d1c267-c55e-4503-b46b-b50894894543
Source feed: FDA_Inspections

> FDA Inspection 1000138 for PRS Medical Technologies Inc. on December 19, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1000138 - 2016-12-19](https://www.keypedia.com/records/fda_inspections/prs-medical-technologies-inc/cb09457c-128e-4840-a134-1ff900b611c5)

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