FDA Inspection 699353 — Versiti Michigan, Inc

Versiti Michigan, Inc — FEI 1000517886

The FDA completed an inspection of Versiti Michigan, Inc on November 18, 2010 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
November 18, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Traverse City, MI (United States)