# Genesys Orthopedics Systems, LLC – FDA Inspection, Sep 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/genesys-orthopedics-systems-llc/c983c277-852e-4d39-9b11-0703d3684538
Source feed: FDA_Inspections

> FDA inspection 1024529 of Genesys Orthopedics Systems, LLC, September 08, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 806. Form 483 issued. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1024529
- Company Name: Genesys Orthopedics Systems, LLC
- Inspection Date: 2017-09-08
- 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: 1

## Related Documents

- FDA Inspection 1221419 - 2023-08-10
- FDA Inspection 1116370 - 2020-01-16
- FDA Inspection 885278 - 2014-06-24
- FDA Inspection 834819 - 2013-06-05
- [FDA Inspection 773496 - 2012-04-02](https://www.keypedia.com/records/fda_inspections/genesys-orthopedics-systems-llc/ca840dab-faf9-4225-bbcf-98ad9968e8b2)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/iris-c-macinnes/5e8d7fef-18d5-453d-82b2-19e8e2897d26)

Company: https://www.keypedia.com/companies/genesys-orthopedics-systems-llc/4a2e433f-1efa-4082-9c1d-61de05e848e7

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