# CCRM Newport Beach Inc, Newport Beach, CA – FDA Inspections

Source: https://www.keypedia.com/companies/ccrm-newport-beach-inc/2940db46-6faf-4a3e-be1b-d45cea0e606e

> Inspection records and compliance data for CCRM Newport Beach Inc in Newport Beach, California. 6 FDA inspections on record, last inspected October 08, 2024.

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## Details

- Name: CCRM Newport Beach Inc
- FEI Number: 3006397636
- Address Line 1: 3501 Jamboree Rd Ste 1100
- City: Newport Beach
- State: California
- Zip Code: 92660
- Country Name: United States
- Address: 3501 Jamboree Rd Ste 1100, Newport Beach, California 92660, United States
- Country: United States

## Related Documents

- FDA Inspection 1252488 - CCRM Newport Beach Inc - 2024-10-08 — source: FDA, date: October 8, 2024
- [FDA Inspection 1252488 - CCRM Newport Beach Inc - 2024-10-08](https://www.keypedia.com/records/fda_inspections/ccrm-newport-beach-inc/659661d0-ccd7-4030-86fa-d89f285cada4) — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2024
- FDA Inspection 1102754 - CCRM Newport Beach Inc - 2019-07-29 — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2019
- FDA Inspection 1102754 - CCRM Newport Beach Inc - 2019-07-29 — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2019
- FDA Inspection 1028800 - CCRM Newport Beach Inc - 2017-09-28 — classification: No Action Indicated (NAI), source: FDA, date: September 28, 2017
- FDA Inspection 1028800 - CCRM Newport Beach Inc - 2017-09-28 — classification: No Action Indicated (NAI), source: FDA, date: September 28, 2017
- [FDA Inspection 930809 - CCRM Newport Beach Inc - 2015-06-19](https://www.keypedia.com/records/fda_inspections/ccrm-newport-beach-inc/3368d3c3-6cc0-40d7-97d6-cd9abcc5a635) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2015
- FDA Inspection 845765 - CCRM Newport Beach Inc - 2013-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2013
- FDA Inspection 704356 - CCRM Newport Beach Inc - 2011-01-06 — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2011

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