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FDA Inspection 648414 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on February 8, 2010 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
February 8, 2010
Fiscal Year
2010
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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  • 1130510 (NAI Fri Sep 04 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066073 (NAI Wed Aug 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984353 (VAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984997 (NAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources