FDA Inspection 1222910 — Adolph V Lombardi MD

Adolph V Lombardi MD — FEI 3006643479

The FDA completed an inspection of Adolph V Lombardi MD on Nov 3, 2023 in New Albany, OH. 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
Nov 3, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New Albany, OH (United States)

Additional Details

Clinical Investigator (CI)

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