FDA Inspection 1061149 — Methodist Women's Hospital

Methodist Women's Hospital — FEI 3008570689

The FDA completed an inspection of Methodist Women's Hospital on Jul 10, 2018 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
Jul 10, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Elkhorn, NE (United States)