# FDA Inspection 1115560 - Genicon, Inc. - January 17, 2020

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

> FDA Inspection 1115560 for Genicon, Inc. on January 17, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1115560
- Company Name: Genicon, Inc.
- Inspection Date: 2020-01-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1115560 - 2020-01-17](https://www.globalkeysolutions.net/records/fda_inspections/genicon-inc/6362c9a1-2154-4368-b027-18d2504e4dc3)
- [FDA Inspection 1029478 - 2017-10-20](https://www.globalkeysolutions.net/records/fda_inspections/genicon-inc/5f7c1671-5e70-450c-a294-2ba380010786)
- [FDA Inspection 1029478 - 2017-10-20](https://www.globalkeysolutions.net/records/fda_inspections/genicon-inc/25d492d8-2efe-424d-8840-d1105072458f)
- [FDA Inspection 923674 - 2015-04-21](https://www.globalkeysolutions.net/records/fda_inspections/genicon-inc/56b72c12-1285-4598-890d-ff6b830cdf0f)
- [FDA Inspection 923674 - 2015-04-21](https://www.globalkeysolutions.net/records/fda_inspections/genicon-inc/dee329ab-881f-4ac1-872f-efd7c0d93f9c)

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

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