# Keystone Dental Inc – FDA Inspection, Jun 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/keystone-dental-inc/f554cbb8-a6e4-4fa8-a6d6-d79b7f60a2df
Source feed: FDA_Inspections

> FDA inspection 1014229 of Keystone Dental Inc, June 08, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014229
- Company Name: Keystone Dental Inc
- Inspection Date: 2017-06-08
- 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: 3

## Related Documents

- FDA Inspection 851881 - 2013-10-07
- [FDA Inspection 797857 - 2012-10-12](https://www.keypedia.com/records/fda_inspections/keystone-dental-inc/34e48030-3c9c-4193-a3dc-c6df717daff8)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/elizabeth-b-griffin/5567685a-c657-4710-afee-e7af8875b605)

Company: https://www.keypedia.com/companies/keystone-dental-inc/6025d413-6f2b-4b7c-a40e-280ceb57ac72

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