# Electro Kinetic Technologies, LLC – FDA Inspection, Jan 17, 2013

Source: https://www.keypedia.com/records/fda_inspections/electro-kinetic-technologies-llc/f19b38aa-f062-4897-a900-3e251abde22e
Source feed: FDA_Inspections

> FDA inspection 815278 of Electro Kinetic Technologies, LLC, January 17, 2013. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 815278
- Company Name: Electro Kinetic Technologies, LLC
- Inspection Date: 2013-01-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- [FDA Inspection 1079466 - 2019-02-15](https://www.keypedia.com/records/fda_inspections/electro-kinetic-technologies-llc/de2b8a56-5cf2-4844-bf3b-1be4a7fc18b3)
- FDA Inspection 861890 - 2014-01-08

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