# Robert R. Mendes MD – FDA Inspection, Mar 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/robert-r-mendes-md/f5f5dbff-f63f-400c-9ab0-e61274e77848
Source feed: FDA_Inspections

> FDA inspection 1004839 of Robert R. Mendes MD, March 08, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004839
- Company Name: Robert R. Mendes MD
- Inspection Date: 2017-03-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1303350 - 2026-02-12
- [FDA Inspection 772407 - 2012-03-09](https://www.keypedia.com/records/fda_inspections/robert-r-mendes-md/af0fbd27-3471-4d4c-a5a0-ac9b8e0531ed)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/betsy-c-galliher/04add63c-cbcb-42f7-b634-7c2925600bef)

Company: https://www.keypedia.com/companies/robert-r-mendes-md/b60cddec-85a1-4053-b454-c38ed7e2453d

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