# FDA Inspection 1035886 - Ronald Luff, MD - December 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/ronald-luff-md/b3db7c28-df51-4e94-a6ed-31aa5797f48c
Source feed: FDA_Inspections

> FDA Inspection 1035886 for Ronald Luff, MD on December 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035886
- Company Name: Ronald Luff, MD
- Inspection Date: 2017-12-19
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/ronald-luff-md/b5be2487-2077-4bd9-92e4-867c71f37c36

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