FDA Inspection 801695 — Albert W. Schreiner III

Albert W. Schreiner III — FEI 3009705314

The FDA completed an inspection of Albert W. Schreiner III on September 28, 2012 in Cincinnati, OH. 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
September 28, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cincinnati, OH (United States)

Additional Details

Clinical Investigator (CI)