FDA Inspection 1247057 — Matthew G. Davis, M.D.

Matthew G. Davis, M.D. — FEI 3007220553

The FDA completed an inspection of Matthew G. Davis, M.D. on August 9, 2024 in Rochester, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 9, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Rochester, NY (United States)

Additional Details

Clinical Investigator (CI)