# Genicon, Inc. – FDA Inspection, Nov 7, 2008

Source: https://www.keypedia.com/records/fda_inspections/genicon-inc/6b878b20-cd7a-4693-9364-eadb5b14127e
Source feed: FDA_Inspections

> FDA inspection 548132 of Genicon, Inc., November 07, 2008. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 548132
- Company Name: Genicon, Inc.
- Inspection Date: 2008-11-07
- 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

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