FDA Inspection 783554 — Larry Blankenship

Larry Blankenship — FEI 3008282269

The FDA completed an inspection of Larry Blankenship on May 15, 2012 in Anderson, IN. 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
May 15, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Anderson, IN (United States)

Additional Details

Clinical Investigator (CI)