FDA Inspection 552692 — Matthew G. Davis, M.D.

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

The FDA completed an inspection of Matthew G. Davis, M.D. on December 11, 2008 in Rochester, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rochester, NY (United States)

Additional Details

Clinical Investigator (CI)