# FDA Inspection 817837 - Robert A. Fernandez, MD - February 08, 2013

Source: https://www.keypedia.com/records/fda_inspections/robert-a-fernandez-md/2fb13f68-574a-4b65-b216-575c352f8a18
Source feed: FDA_Inspections

> FDA Inspection 817837 for Robert A. Fernandez, MD on February 08, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817837
- Company Name: Robert A. Fernandez, MD
- Inspection Date: 2013-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/robert-a-fernandez-md/69727d63-aaf7-488f-82a8-232f6a81171e

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