FDA Inspection 614760 — Edward M. Kerwin, M.D

Edward M. Kerwin, M.D — FEI 3003591924

The FDA completed an inspection of Edward M. Kerwin, M.D on September 18, 2009 in Medford, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 18, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Medford, OR (United States)

Additional Details

Clinical Investigator (CI)