FDA Inspection 1300384 — Oliver M. Barry, MD

Oliver M. Barry, MD — FEI 3041226438

The FDA completed an inspection of Oliver M. Barry, MD on December 12, 2025 in New York, NY. 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
December 12, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New York, NY (United States)

Additional Details

Clinical Investigator (CI)