FDA Inspection 699353 — Versiti Michigan, Inc

Versiti Michigan, Inc — FEI 1000517886

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

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