FDA Inspection 836858 — Edward M. Kerwin, M.D

Edward M. Kerwin, M.D — FEI 3003591924

The FDA completed an inspection of Edward M. Kerwin, M.D on June 20, 2013 in Medford, OR. 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
June 20, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Medford, OR (United States)

Additional Details

Clinical Investigator (CI)