FDA Inspection 989871 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 3008141702

The FDA completed an inspection of Versiti Michigan Inc on October 25, 2016 in Portage, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 25, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portage, MI (United States)