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FDA Inspection
•Dynatronics Corp Chattanooga Operations•May 10, 2017

Dynatronics Corp Chattanooga Operations – FDA Inspection, May 10, 2017

Record Details

This FDA Inspection record concerns Dynatronics Corp Chattanooga Operations, with an inspection on May 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Dynatronics Corp Chattanooga Operations
Inspection Date
May 10, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Andrew Saunders
View Company Profile

ID · b4a45ab4-64b0-4c62-99a7-6efb1d2f5c5d

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1019365
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.184DHR content
  2. 21 CFR 820.198(e)Records of complaint investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Dynatronics Corp Chattanooga Operations

3
DateClassificationOfficeProject area
March 10, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 23, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
September 8, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Dynatronics Corp Chattanooga Operations
  • FDA Inspection 917358 - 2015-03-10
  • FDA Inspection 783513 - 2012-05-23
  • FDA Inspection 610719 - 2009-09-08

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