FDA Inspection 1281155 — Robert J. Hayashi, MD

Robert J. Hayashi, MD — FEI 3022205731

The FDA completed an inspection of Robert J. Hayashi, MD on August 29, 2025 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)