FDA Inspection 553031 — Ernie Riffer MD

Ernie Riffer MD — FEI 3003354534

The FDA completed an inspection of Ernie Riffer MD on December 18, 2008 in Phoenix, AZ. 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
December 18, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)