# Rhinosystems Inc – FDA Inspection, Feb 8, 2024

Source: https://www.keypedia.com/records/fda_inspections/rhinosystems-inc/a16a3976-87b0-4693-bcdd-90c10a20f7b5
Source feed: FDA_Inspections

> FDA inspection 1228863 of Rhinosystems Inc, February 08, 2024. Classification: Voluntary Action Indicated (VAI). 4 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: 1228863
- Company Name: Rhinosystems Inc
- Inspection Date: 2024-02-08
- 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: 4

## Related Documents

- [FDA Inspection 996259 - 2016-12-02](https://www.keypedia.com/records/fda_inspections/rhinosystems-inc/bcaab9a8-6c2a-44cd-af86-47c2d726ba01)
- FDA Inspection 649782 - 2010-03-04

## Related Officers

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

Company: https://www.keypedia.com/companies/rhinosystems-inc/ab2597a6-c92c-447d-9b95-09dffcd22802

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