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FDA Inspection 1030666 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 3005861846

The FDA completed an inspection of Versiti Michigan Inc on October 25, 2017 in Saint Joseph, 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
October 25, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Joseph, MI (United States)

Facility

Other inspections at this facility

  • 1106609 (NAI Wed Oct 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 958137 (NAI Wed Dec 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859621 (NAI Tue Dec 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 759627 (NAI Tue Dec 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 631166 (NAI Wed Nov 25 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources