FDA Inspection 558852 — Versiti Michigan, Inc

Versiti Michigan, Inc — FEI 1000517886

The FDA completed an inspection of Versiti Michigan, Inc on January 15, 2009 in Traverse City, 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
January 15, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Traverse City, MI (United States)