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FDA Inspection 912981 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 3008141702

The FDA completed an inspection of Versiti Michigan Inc on December 23, 2014 in Portage, 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 23, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portage, MI (United States)

Facility

Other inspections at this facility

  • 1219070 (NAI Fri Sep 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1080678 (NAI Mon Feb 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 989871 (NAI Tue Oct 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 820928 (NAI Tue Mar 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710920 (NAI Tue Feb 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources