# CIT Ortho – FDA Inspection, Sep 5, 2023

Source: https://www.keypedia.com/records/fda_inspections/cit-ortho/51e5e26b-efb3-4344-9fb2-b8c465f15a64
Source feed: FDA_Inspections

> FDA inspection 1216856 of CIT Ortho, September 05, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216856
- Company Name: CIT Ortho
- Inspection Date: 2023-09-05
- 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: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

Company: https://www.keypedia.com/companies/cit-ortho/7b882ff6-5a8f-48e4-8f98-64b9b2a43b40

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