# Continental Dental Ceramics Inc. - Inspection Records

Source: https://www.keypedia.com/companies/continental-dental-ceramics-inc/f05bd280-85ac-43ae-ae22-e1ce79841cd0

> Inspection records and compliance data for Continental Dental Ceramics Inc. in Torrance, California. Access full analysis and detailed observations.

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## Details

- Name: Continental Dental Ceramics Inc.
- FEI Number: 3004146605
- City: Torrance
- State: California
- Country Name: United States
- Address Line 1: 1873 Western Way
- Zip Code: 90501

## Related Documents

- [483 - Continental Dental Ceramics Inc. - 2022-07-15](https://www.keypedia.com/records/483/continental-dental-ceramics-inc/e53eb746-6ce4-4161-b5e8-6bfaf055bde0) — source: FDA, date: July 15, 2022
- [FDA Inspection 1177606 - Continental Dental Ceramics Inc. - 2022-07-15](https://www.keypedia.com/records/fda_inspections/continental-dental-ceramics-inc/aae2ee16-5a5d-4620-b3d4-5f69c029331b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2022
- [FDA Inspection 1177606 - Continental Dental Ceramics Inc. - 2022-07-15](https://www.keypedia.com/records/fda_inspections/continental-dental-ceramics-inc/710c74af-6ad7-416c-95a9-8bec04083263) — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2022
- [FDA Inspection 990443 - Continental Dental Ceramics Inc. - 2016-07-20](https://www.keypedia.com/records/fda_inspections/continental-dental-ceramics-inc/785e3ae3-7b60-418f-a3f5-41baba699267) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2016
- [FDA Inspection 768738 - Continental Dental Ceramics Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/continental-dental-ceramics-inc/a54d17f8-983a-4565-86ff-e97575d0842f) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012
- [FDA Inspection 768738 - Continental Dental Ceramics Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/continental-dental-ceramics-inc/488b33d3-d76b-4231-b3b5-6d22541e2366) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012

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