FDA Inspection 1306620 — Mark Galantowicz, MD

Mark Galantowicz, MD — FEI 3041227582

The FDA completed an inspection of Mark Galantowicz, MD on February 27, 2026 in Columbus, OH. 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 27, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Columbus, OH (United States)

Additional Details

Clinical Investigator (CI)