# Reflexonic, LLC – FDA Inspection, Oct 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/reflexonic-llc/9cf57c7c-0b12-46e2-bbda-c7426ed1d5af
Source feed: FDA_Inspections

> FDA inspection 1069061 of Reflexonic, LLC, October 17, 2018. Classification: Voluntary Action Indicated (VAI). 14 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069061
- Company Name: Reflexonic, LLC
- Inspection Date: 2018-10-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 14

## Related Documents

- [FDA Inspection 1283212 - 2025-09-24](https://www.keypedia.com/records/fda_inspections/reflexonic-llc/6c370d33-ee5c-4d9f-bd4f-13ca8bdc19f1)
- [FDA Inspection 968449 - 2016-04-19](https://www.keypedia.com/records/fda_inspections/reflexonic-llc/9535bc86-2ae8-4581-aef4-9b856e1dc5a4)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)
- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

Company: https://www.keypedia.com/companies/reflexonic-llc/5573866a-b9b9-4844-8a5a-54641b8125d4

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