FDA Inspection 830397 — Edward M. Kerwin, M.D

Edward M. Kerwin, M.D — FEI 3003591924

The FDA completed an inspection of Edward M. Kerwin, M.D on October 17, 2012 in Medford, OR. 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
October 17, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Medford, OR (United States)

Additional Details

Clinical Investigator (CI)