FDA Inspection 1119492 — Loukas S. Boutis, MD

Loukas S. Boutis, MD — FEI 3016239179

The FDA completed an inspection of Loukas S. Boutis, MD on February 7, 2020 in Manhasset, 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
February 7, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Manhasset, NY (United States)

Additional Details

Clinical Investigator (CI)