FDA Inspection 957137 — Methodist Women's Hospital

Methodist Women's Hospital — FEI 3008570689

The FDA completed an inspection of Methodist Women's Hospital on Jan 26, 2016 in Elkhorn, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 26, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Elkhorn, NE (United States)