FDA Inspection 1252371 — Arvin George, M.D.

Arvin George, M.D. — FEI 3030989594

The FDA completed an inspection of Arvin George, M.D. on Oct 9, 2024 in Ann Arbor, MI. 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
Oct 9, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Ann Arbor, MI (United States)

Additional Details

Clinical Investigator (CI)

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