FDA Inspection 1041339 — Edward M. Kerwin, M.D

Edward M. Kerwin, M.D — FEI 3003591924

The FDA completed an inspection of Edward M. Kerwin, M.D on January 19, 2018 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
January 19, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Medford, OR (United States)

Additional Details

In Vivo Bioequivalence