FDA Inspection 930498 — Versiti Michigan, Inc

Versiti Michigan, Inc — FEI 1000517886

The FDA completed an inspection of Versiti Michigan, Inc on June 17, 2015 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
June 17, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Traverse City, MI (United States)