# Reflexonic, LLC – FDA Inspection, Apr 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/reflexonic-llc/9535bc86-2ae8-4581-aef4-9b856e1dc5a4
Source feed: FDA_Inspections

> FDA inspection 968449 of Reflexonic, LLC, April 19, 2016. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 968449
- Company Name: Reflexonic, LLC
- Inspection Date: 2016-04-19
- 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: 9

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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