Home / Inspections / 855918

FDA Inspection 855918 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 3005010959

The FDA completed an inspection of Versiti Illinois Inc on October 29, 2013 in Dekalb, IL. 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
October 29, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dekalb, IL (United States)

Facility

Other inspections at this facility

  • 1260010 (NAI Wed Jan 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1106927 (NAI Tue Sep 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025429 (NAI Mon Aug 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 916787 (NAI Thu Mar 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 772491 (NAI Tue Feb 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources