# Genicon, Inc. – FDA Inspection, Oct 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/genicon-inc/5f7c1671-5e70-450c-a294-2ba380010786
Source feed: FDA_Inspections

> FDA inspection 1029478 of Genicon, Inc., October 20, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029478
- Company Name: Genicon, Inc.
- Inspection Date: 2017-10-20
- 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: 5

## Related Documents

- [FDA Inspection 1115560 - 2020-01-17](https://www.keypedia.com/records/fda_inspections/genicon-inc/a21d65bc-f713-40dc-b86a-c87b4c7bb75b)
- FDA Inspection 923674 - 2015-04-21
- FDA Inspection 775196 - 2012-03-29
- [FDA Inspection 548132 - 2008-11-07](https://www.keypedia.com/records/fda_inspections/genicon-inc/6b878b20-cd7a-4693-9364-eadb5b14127e)

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/genicon-inc/d7897305-74e7-4ce7-8b68-558f883e2478

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