# FDA Inspection 1258640 - Santiago Ortega Gutierrez, M.D. - January 17, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/santiago-ortega-gutierrez-md/bf5b0637-7dbd-471a-8541-9a616aeed63e
Source feed: FDA_Inspections

> FDA Inspection 1258640 for Santiago Ortega Gutierrez, M.D. on January 17, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258640
- Company Name: Santiago Ortega Gutierrez, M.D.
- Inspection Date: 2025-01-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1310990 - 2026-03-27](https://www.globalkeysolutions.net/records/fda_inspections/santiago-ortega-gutierrez-md/76acb76a-c8d6-4965-aa4e-107fc70d8682)
- [FDA Inspection 1258640 - 2025-01-17](https://www.globalkeysolutions.net/records/fda_inspections/santiago-ortega-gutierrez-md/2559a789-7ac6-42cc-b93b-bf0d2b0f1bd4)

Company: https://www.globalkeysolutions.net/companies/santiago-ortega-gutierrez-md/133920d8-6a6e-4b53-bd64-ead1b01b5ab5

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7