# Crystalmark Dental Systems Inc, Glendale, CA – FDA Inspections

Source: https://www.keypedia.com/companies/crystalmark-dental-systems-inc/e6629cff-f33f-4fff-9758-eee972ad8ffa

> Inspection records and compliance data for Crystalmark Dental Systems Inc in Glendale, California. 4 FDA inspections on record, last inspected October 22, 2021.

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## Details

- Name: Crystalmark Dental Systems Inc
- FEI Number: 1000306507
- Address Line 1: 621 Ruberta Ave Ste 1
- City: Glendale
- State: California
- Zip Code: 91201
- Country Name: United States
- Address: 621 Ruberta Ave Ste 1, Glendale, California 91201, United States
- Country: United States

## Related Documents

- [483 - Crystalmark Dental Systems Inc - 2021-10-22](https://www.keypedia.com/records/483/crystalmark-dental-systems-inc/2ed64016-4c3a-431d-b727-e7796368bd9c) — source: FDA, date: October 22, 2021
- FDA Inspection 1156979 - Crystalmark Dental Systems Inc - 2021-10-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2021
- FDA Inspection 1156979 - Crystalmark Dental Systems Inc - 2021-10-22 — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2021
- FDA Inspection 1070376 - Crystalmark Dental Systems Inc - 2018-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2018
- FDA Inspection 1070376 - Crystalmark Dental Systems Inc - 2018-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2018
- FDA Inspection 863194 - Crystalmark Dental Systems Inc - 2014-01-21 — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2014
- FDA Inspection 863194 - Crystalmark Dental Systems Inc - 2014-01-21 — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2014
- FDA Inspection 744675 - Crystalmark Dental Systems Inc - 2011-09-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2011
- FDA Inspection 744675 - Crystalmark Dental Systems Inc - 2011-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2011

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