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FDA Inspection 1080678 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 3008141702

The FDA completed an inspection of Versiti Michigan Inc on February 11, 2019 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
February 11, 2019
Fiscal Year
2019
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))
  • 989871 (NAI Tue Oct 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 912981 (NAI Tue Dec 23 2014 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