FDA Inspection 793048 — Jungbluth, Deanne

Jungbluth, Deanne — FEI 3009562359

The FDA completed an inspection of Jungbluth, Deanne on Aug 1, 2012 in Saint Joseph, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 1, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Saint Joseph, MO (United States)

Additional Details

Clinical Investigator (CI)