# FDA Inspection 1004839 - Robert R. Mendes MD - March 08, 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 for Robert R. Mendes MD on March 08, 2017. Classification: No Action Indicated (NAI).

---

## Details

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

## Related Documents

- [FDA Inspection 1303350 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/robert-r-mendes-md/3839ef12-cf5e-40e9-a18b-be04fa7a3cd6)
- [FDA Inspection 1303350 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/robert-r-mendes-md/05293002-9ac1-46cf-86fa-ead1992437c7)
- [FDA Inspection 772407 - 2012-03-09](https://www.keypedia.com/records/fda_inspections/robert-r-mendes-md/af0fbd27-3471-4d4c-a5a0-ac9b8e0531ed)

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
