FDA Inspection 1334006 — Alexis M. Cahalane, M.D.

Alexis M. Cahalane, M.D. — FEI 3045078087

The FDA completed an inspection of Alexis M. Cahalane, M.D. on Aug 20, 2026 in Boston, MA. 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
Aug 20, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Boston, MA (United States)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.