FDA Inspection 1101500 — Ralph A. Liebelt, M.D.

Ralph A. Liebelt, M.D. — FEI 3004989093

The FDA completed an inspection of Ralph A. Liebelt, M.D. on August 21, 2019 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Durham, NC (United States)

Additional Details

Clinical Investigator (CI)