# Dynatronics Corporation – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/dynatronics-corporation/b27980a0-3f1e-4f94-833f-fec997d5c08c
Source feed: FDA_Inspections

> FDA inspection 1031095 of Dynatronics Corporation, November 09, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031095
- Company Name: Dynatronics Corporation
- Inspection Date: 2017-11-09
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1218746 - 2023-09-19
- [FDA Inspection 911037 - 2015-01-16](https://www.keypedia.com/records/fda_inspections/dynatronics-corporation/7f657682-8c0e-4d26-990b-9a61612cefcf)
- FDA Inspection 739475 - 2011-08-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/dynatronics-corporation/0c5d6b0f-b453-481b-99f4-44270ad63179

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