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FDA Inspection 878357 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on May 9, 2014 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
May 9, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1245903 (NAI Thu Jun 27 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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