FDA Inspection 973595 — Anne Luetkemeyer

Anne Luetkemeyer — FEI 3012014526

The FDA completed an inspection of Anne Luetkemeyer on May 12, 2016 in San Francisco, CA. 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 12, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Francisco, CA (United States)

Additional Details

Clinical Investigator (CI)