# FDA Inspection 695543 - Gendex Dental Systems - October 08, 2010

Source: https://www.keypedia.com/records/fda_inspections/gendex-dental-systems/a99d363c-6c10-4df5-ab87-6014b56c39b1
Source feed: FDA_Inspections

> FDA Inspection 695543 for Gendex Dental Systems on October 08, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695543
- Company Name: Gendex Dental Systems
- Inspection Date: 2010-10-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 695543 - 2010-10-08](https://www.keypedia.com/records/fda_inspections/gendex-dental-systems/09417f5d-f8c0-406f-9bd2-80b37182887a)
- [FDA Inspection 695543 - 2010-10-08](https://www.keypedia.com/records/fda_inspections/gendex-dental-systems/b95092c2-12f8-44e6-b9cc-cacb21c0f850)
- [FDA Inspection 600329 - 2009-05-06](https://www.keypedia.com/records/fda_inspections/gendex-dental-systems/284bc11c-db56-4eee-9daf-e27e9e176ab8)

Company: https://www.keypedia.com/companies/gendex-dental-systems/371ed051-d1bc-4f49-a431-e206b6fb3490

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