FDA Inspection 1335584 — Ralph Cutler Quillin III, MD

Ralph Cutler Quillin III, MD — FEI 3046004635

The FDA completed an inspection of Ralph Cutler Quillin III, MD on Aug 21, 2026 in Cincinnati, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 21, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Cincinnati, OH (United States)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.