# FDA Inspection 836092 - Pulpdent Corporation - June 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/7033c8bd-7cd3-464d-b4d9-c2138a64a558
Source feed: FDA_Inspections

> FDA Inspection 836092 for Pulpdent Corporation on June 11, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 836092
- Company Name: Pulpdent Corporation
- Inspection Date: 2013-06-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 709225 - 2011-02-08](https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/41d9355d-e589-4532-a9df-55eed33483e4)
- [FDA Inspection 577342 - 2009-04-17](https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/8bca3ed2-836e-4aa5-8fa2-0ac7da4db3cf)

Company: https://www.keypedia.com/companies/pulpdent-corporation/5281d2aa-860f-4197-b38e-3a80fe7f5d60

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