# Electro Kinetic Technologies, LLC – FDA Inspection, Feb 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/electro-kinetic-technologies-llc/de2b8a56-5cf2-4844-bf3b-1be4a7fc18b3
Source feed: FDA_Inspections

> FDA inspection 1079466 of Electro Kinetic Technologies, LLC, February 15, 2019. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079466
- Company Name: Electro Kinetic Technologies, LLC
- Inspection Date: 2019-02-15
- 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: 1

## Related Documents

- FDA Inspection 861890 - 2014-01-08
- [FDA Inspection 815278 - 2013-01-17](https://www.keypedia.com/records/fda_inspections/electro-kinetic-technologies-llc/f19b38aa-f062-4897-a900-3e251abde22e)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)

Company: https://www.keypedia.com/companies/electro-kinetic-technologies-llc/a9582b99-3978-44d1-8e57-cbc54dc045d0

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