# SSM Cardinal Glennon Childrens Hospital - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ssm-cardinal-glennon-childrens-hospital/482a8706-cea4-4ff4-bdd4-9bf30b78e4da

> Inspection records and compliance data for SSM Cardinal Glennon Childrens Hospital in Saint Louis, Missouri. Access full analysis and detailed observations.

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## Details

- Name: SSM Cardinal Glennon Childrens Hospital
- FEI Number: 1970727
- City: Saint Louis
- State: Missouri
- Country Name: United States
- Address Line 1: 1465 S Grand Blvd
- Zip Code: 63104

## Related Documents

- [FDA Inspection 1078250 - SSM Cardinal Glennon Childrens Hospital - 2019-01-29](https://www.globalkeysolutions.net/records/fda_inspections/ssm-cardinal-glennon-childrens-hospital/19cfb586-7c33-4a35-8a9d-d0e0deb72dcc) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2019
- [FDA Inspection 991440 - SSM Cardinal Glennon Childrens Hospital - 2016-11-02](https://www.globalkeysolutions.net/records/fda_inspections/ssm-cardinal-glennon-childrens-hospital/03d870fe-3c2b-4b3c-b46d-a72c2c5b6fde) — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2016
- [FDA Inspection 904375 - SSM Cardinal Glennon Childrens Hospital - 2014-11-20](https://www.globalkeysolutions.net/records/fda_inspections/ssm-cardinal-glennon-childrens-hospital/fb0fa128-700a-49b8-a42e-0d599f7c6547) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2014
- [FDA Inspection 837088 - SSM Cardinal Glennon Childrens Hospital - 2013-03-19](https://www.globalkeysolutions.net/records/fda_inspections/ssm-cardinal-glennon-childrens-hospital/ae60660c-2439-474d-9d27-c849654b5514) — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2013
- [FDA Inspection 661056 - SSM Cardinal Glennon Childrens Hospital - 2010-05-11](https://www.globalkeysolutions.net/records/fda_inspections/ssm-cardinal-glennon-childrens-hospital/6c116058-f01d-4f33-91c3-ea983f0766e5) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2010

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