# Mission Hospital Regional Medical Center, Mission Viejo, CA – FDA Inspections

Source: https://www.keypedia.com/companies/mission-hospital-regional-medical-center/d4d872c7-a5f3-4b2c-aa6e-21330b936291

> Inspection records and compliance data for Mission Hospital Regional Medical Center in Mission Viejo, California. 7 FDA inspections on record, 1 Form 483, last inspected August 15, 2024.

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## Details

- Name: Mission Hospital Regional Medical Center
- FEI Number: 2077909
- Address Line 1: 27700 Medical Center Rd
- City: Mission Viejo
- State: California
- Zip Code: 92691
- Country Name: United States
- Address: 27700 Medical Center Rd, Mission Viejo, California 92691, United States
- Country: United States

## Related Documents

- FDA Inspection 1249306 - Mission Hospital Regional Medical Center - 2024-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2024
- [FDA Inspection 1078101 - Mission Hospital Regional Medical Center - 2019-02-04](https://www.keypedia.com/records/fda_inspections/mission-hospital-regional-medical-center/a1468944-f208-4b0e-9984-3e10efe46d90) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 4, 2019
- FDA Inspection 1009001 - Mission Hospital Regional Medical Center - 2017-03-13 — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2017
- FDA Inspection 950100 - Mission Hospital Regional Medical Center - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 867128 - Mission Hospital Regional Medical Center - 2014-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2014
- [FDA Inspection 777258 - Mission Hospital Regional Medical Center - 2012-04-17](https://www.keypedia.com/records/fda_inspections/mission-hospital-regional-medical-center/91c0ea68-633e-4b33-9e38-31859e63d937) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2012
- FDA Inspection 681198 - Mission Hospital Regional Medical Center - 2010-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2010

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