FDA Inspection 1009630 — Andreas Reiter, M.D.

Andreas Reiter, M.D. — FEI 3012811360

The FDA completed an inspection of Andreas Reiter, M.D. on January 27, 2017 in Mannheim. 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 27, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Clinical Investigator (CI)