# Ultradent Products, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ultradent-products-inc/16b4d8af-54bd-48d3-acc8-a5169bd5bfe3

> Inspection records and compliance data for Ultradent Products, Inc. in South Jordan, Utah. Access full analysis and detailed observations.

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## Details

- Name: Ultradent Products, Inc.
- FEI Number: 1718912
- City: South Jordan
- State: Utah
- Country Name: United States
- Address Line 1: 505 W 10200 S
- Zip Code: 84095

## Related Documents

- [483 - Ultradent Products, Inc. - 2025-06-13](https://www.globalkeysolutions.net/records/483/ultradent-products-inc/a610038b-335f-4096-9fea-006239a00b62) — source: FDA, date: June 13, 2025
- [FDA Inspection 1272589 - Ultradent Products, Inc. - 2025-06-13](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/18c20140-ee87-4c83-9724-258022b594ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2025
- [483 - Ultradent Products, Inc. - 2020-01-17](https://www.globalkeysolutions.net/records/483/ultradent-products-inc/a637303d-272f-4c64-978e-db982ba91455) — source: FDA, date: January 17, 2020
- [FDA Inspection 1115289 - Ultradent Products, Inc. - 2020-01-17](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/66fe3028-a4fc-4780-a727-51a288d5f55d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 17, 2020
- [FDA Inspection 1086182 - Ultradent Products, Inc. - 2019-03-28](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/1457ec33-dabc-4f33-91aa-87241da70a49) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2019
- [FDA Inspection 1086182 - Ultradent Products, Inc. - 2019-03-28](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/3a4f8f43-17e7-4d0f-9c95-028c1fceacc6) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2019
- [483 - Ultradent Products, Inc. - 2017-09-15](https://www.globalkeysolutions.net/records/483/ultradent-products-inc/bac4444e-d4c5-4ce4-bd25-14624d8ccdd6) — source: FDA, date: September 15, 2017
- [FDA Inspection 1025250 - Ultradent Products, Inc. - 2017-09-15](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/f53c1f50-8e3a-4190-9346-3baafd7f0a1e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2017
- [FDA Inspection 895359 - Ultradent Products, Inc. - 2014-09-12](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/e44bb129-c255-44d7-9a1e-b9fd4a5c7066) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2014
- [FDA Inspection 895359 - Ultradent Products, Inc. - 2014-09-12](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/8df16314-e11a-4c91-bed7-1e025245df91) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2014
- [FDA Inspection 895359 - Ultradent Products, Inc. - 2014-09-12](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/01a30b51-bf6f-447c-89bc-88d3ab39986a) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2014
- [WARNING_LETTER - Ultradent Products, Inc. - 2013-11-08](https://www.globalkeysolutions.net/records/warning_letter/ultradent-products-inc/b7b9bccc-0106-4a34-8214-01c437142f8f) — source: FDA, date: November 8, 2013
- [FDA Inspection 854539 - Ultradent Products, Inc. - 2013-11-08](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/8ab7257e-3207-410d-adac-4b192f613967) — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2013
- [FDA Inspection 854539 - Ultradent Products, Inc. - 2013-11-08](https://www.globalkeysolutions.net/records/fda_inspections/ultradent-products-inc/9ea95e2a-6a6c-4de8-a98c-40a5b36047ff) — classification: Official Action Indicated (OAI), source: FDA, date: November 8, 2013

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