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FDA Inspection 960526 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1876521

The FDA completed an inspection of Versiti Michigan Inc on January 25, 2016 in Bay City, 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
January 25, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bay City, MI (United States)

Facility

Other inspections at this facility

  • 1251179 (NAI Wed Sep 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1117466 (NAI Thu Jan 09 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1034547 (NAI Wed Oct 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 862246 (NAI Wed Jan 15 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767164 (NAI Mon Jan 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources