# Orthoessentials – FDA Inspection, Feb 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/orthoessentials/eb1482e5-67e7-414d-bbb5-651a43000ddc
Source feed: FDA_Inspections

> FDA inspection 1000574 of Orthoessentials, February 08, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000574
- Company Name: Orthoessentials
- Inspection Date: 2017-02-08
- 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: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/meredith-l-sheridan/4021bfe4-3d32-44da-8dc2-e85d1807c000)

Company: https://www.keypedia.com/companies/orthoessentials/65e9b792-0e68-4d1b-ac65-a7ce8c69693e

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