# FDA Inspection 1069061 - Reflexonic, LLC - October 17, 2018

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

> FDA Inspection 1069061 for Reflexonic, LLC on October 17, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

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

## Related Documents

- [FDA Inspection 1283212 - 2025-09-24](https://www.globalkeysolutions.net/records/fda_inspections/reflexonic-llc/59e8ead8-dce3-4fa0-8a3a-17855c88a29d)
- [FDA Inspection 1283212 - 2025-09-24](https://www.globalkeysolutions.net/records/fda_inspections/reflexonic-llc/6c370d33-ee5c-4d9f-bd4f-13ca8bdc19f1)
- [FDA Inspection 1069061 - 2018-10-17](https://www.globalkeysolutions.net/records/fda_inspections/reflexonic-llc/994dfad9-8402-422d-a7ae-7e6ea29fe8e9)
- [FDA Inspection 968449 - 2016-04-19](https://www.globalkeysolutions.net/records/fda_inspections/reflexonic-llc/7a9d430d-00df-4c6b-9001-0fa9acc80ed0)
- [FDA Inspection 968449 - 2016-04-19](https://www.globalkeysolutions.net/records/fda_inspections/reflexonic-llc/9535bc86-2ae8-4581-aef4-9b856e1dc5a4)

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

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