# Genicon, Inc. – FDA Inspection, Jan 17, 2020

Source: https://www.keypedia.com/records/fda_inspections/genicon-inc/a21d65bc-f713-40dc-b86a-c87b4c7bb75b
Source feed: FDA_Inspections

> FDA inspection 1115560 of Genicon, Inc., January 17, 2020. Classification: Voluntary Action Indicated (VAI). 15 citations under 21 CFR parts 803, 806 and 820. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1115560
- Company Name: Genicon, Inc.
- Inspection Date: 2020-01-17
- 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: 15

## Related Documents

- [FDA Inspection 1029478 - 2017-10-20](https://www.keypedia.com/records/fda_inspections/genicon-inc/5f7c1671-5e70-450c-a294-2ba380010786)
- 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)

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