FDA Inspection
Dynatronics CorporationDynatronics Corporation – FDA Inspection, Nov 9, 2017
Record Details
This FDA Inspection record concerns Dynatronics Corporation, with an inspection on November 9, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b27980a0-3f1e-4f94-833f-fec997d5c08c
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1031095
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Dynatronics Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 19, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 16, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 11, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Dynatronics Corporation
- FDA Inspection 1218746 - 2023-09-19
- FDA Inspection 911037 - 2015-01-16
- FDA Inspection 739475 - 2011-08-11
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