FDA Inspection 1269733 — Andrew Leuchter, M.D.

Andrew Leuchter, M.D. — FEI 3037328041

The FDA completed an inspection of Andrew Leuchter, M.D. on May 12, 2025 in Los Angeles, CA. 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
May 12, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Los Angeles, CA (United States)

Additional Details

Clinical Investigator (CI)