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FDA Inspection 1130510 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on September 4, 2020 in Grand Rapids, 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
September 4, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1245903 (NAI Thu Jun 27 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066073 (NAI Wed Aug 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984353 (VAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984997 (NAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 878357 (NAI Fri May 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources