# Rhinosystems Inc – FDA Inspection, Dec 2, 2016

Source: https://www.keypedia.com/records/fda_inspections/rhinosystems-inc/bcaab9a8-6c2a-44cd-af86-47c2d726ba01
Source feed: FDA_Inspections

> FDA inspection 996259 of Rhinosystems Inc, December 02, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996259
- Company Name: Rhinosystems Inc
- Inspection Date: 2016-12-02
- 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 Documents

- [FDA Inspection 1228863 - 2024-02-08](https://www.keypedia.com/records/fda_inspections/rhinosystems-inc/a16a3976-87b0-4693-bcdd-90c10a20f7b5)
- FDA Inspection 649782 - 2010-03-04

## Related Officers

- Issuing Officer

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