FDA Inspection 917453 — Matthew G. Davis, M.D.

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

The FDA completed an inspection of Matthew G. Davis, M.D. on March 11, 2015 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
March 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Rochester, NY (United States)

Additional Details

Clinical Investigator (CI)