# FDA Inspection 1040021 - Mauricio A. Villavicencio-Theoduloz, MD - December 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/mauricio-a-villavicencio-theoduloz-md/06193201-4da6-4160-b8b7-51f154047d3a
Source feed: FDA_Inspections

> FDA Inspection 1040021 for Mauricio A. Villavicencio-Theoduloz, MD on December 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040021
- Company Name: Mauricio A. Villavicencio-Theoduloz, MD
- Inspection Date: 2017-12-22
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1073138 - 2018-11-07](https://www.keypedia.com/records/fda_inspections/mauricio-a-villavicencio-theoduloz-md/19bcb005-6ace-4a0f-b2fa-076685ee2096)

Company: https://www.keypedia.com/companies/mauricio-a-villavicencio-theoduloz-md/6a750ae3-f4cf-4ed3-8dd4-8ef6b9c9e115

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