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FDA Inspection 759640 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on December 16, 2011 in Grand Rapids, 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
December 16, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

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  • 984353 (VAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources