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FDA Inspection 656009 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1876521

The FDA completed an inspection of Versiti Michigan Inc on April 5, 2010 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
April 5, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bay City, MI (United States)

Facility

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  • 1034547 (NAI Wed Oct 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 960526 (NAI Mon Jan 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 862246 (NAI Wed Jan 15 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources