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FDA Inspection 1090660 — Innovative Blood Resources

Innovative Blood Resources — FEI 2177724

The FDA completed an inspection of Innovative Blood Resources on May 1, 2019 in Duluth, MN. 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
May 1, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Duluth, MN (United States)

Facility

Other inspections at this facility

  • 1252735 (NAI Tue Oct 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025776 (NAI Thu Aug 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928480 (NAI Fri May 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810856 (NAI Wed Feb 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 730719 (NAI Thu Jun 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources