# FDA Inspection 830663 - tulsa dental products llc  - May 03, 2013

Source: https://www.keypedia.com/records/fda_inspections/tulsa-dental-products-llc/d8691342-d83c-4e4d-83b7-f8e47303cd46
Source feed: FDA_Inspections

> FDA Inspection 830663 for tulsa dental products llc  on May 03, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830663
- Company Name: tulsa dental products llc 
- Inspection Date: 2013-05-03
- 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 830663 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/tulsa-dental-products-llc/0de846ce-0302-422c-8c67-0b089ef95595)
- [FDA Inspection 599742 - 2009-05-28](https://www.keypedia.com/records/fda_inspections/tulsa-dental-products-llc/858a3495-e3e3-432e-8d89-dc4525f5f73f)

Company: https://www.keypedia.com/companies/tulsa-dental-products-llc/8d68370a-cf6d-4e42-96c2-fefc46fe431d

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