FDA Inspection 1238036 — Howard Lantner, M.D.

Howard Lantner, M.D. — FEI 3030295088

The FDA completed an inspection of Howard Lantner, M.D. on Apr 29, 2024 in Bloomfield, CT. 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
Apr 29, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bloomfield, CT (United States)

Additional Details

Clinical Investigator (CI)