# Santiago Ortega Gutierrez, M.D. – FDA Inspection, Jan 17, 2025

Source: https://www.keypedia.com/records/fda_inspections/santiago-ortega-gutierrez-md/2559a789-7ac6-42cc-b93b-bf0d2b0f1bd4
Source feed: FDA_Inspections

> FDA inspection 1258640 of Santiago Ortega Gutierrez, M.D., January 17, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Kansas City District Office
- Citation Count: 3

## Related Documents

- FDA Inspection 1310990 - 2026-03-27

## Related Officers

- [Investigator](https://www.keypedia.com/people/logan-m-jones/286ab813-461a-4bfc-a732-bcd4f0d6e596)

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

Office: https://www.keypedia.com/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79