FDA Inspection 1102000 — Patrick J. Denard, MD

Patrick J. Denard, MD — FEI 3015516306

The FDA completed an inspection of Patrick J. Denard, MD on August 28, 2019 in Medford, OR. 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 28, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Medford, OR (United States)

Additional Details

Clinical Investigator (CI)