FDA Inspection 1301590 — Michael G. Moront MD

Michael G. Moront MD — FEI 3013321943

The FDA completed an inspection of Michael G. Moront MD on January 12, 2026 in Toledo, OH. 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
January 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Toledo, OH (United States)

Additional Details

Clinical Investigator (CI)