FDA Inspection 1039579 — Alvadore Osborn, D.O.

Alvadore Osborn, D.O. — FEI 3013934842

The FDA completed an inspection of Alvadore Osborn, D.O. on December 14, 2017 in West Des Moines, IA. 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 14, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
West Des Moines, IA (United States)

Additional Details

Clinical Investigator (CI)