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FDA Inspection 998562 — Versiti Illinois Inc

Versiti Illinois Inc — FEI 1470340

The FDA completed an inspection of Versiti Illinois Inc on January 5, 2017 in Tinley Park, 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
January 5, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tinley Park, IL (United States)

Facility

Other inspections at this facility

  • 1244621 (NAI Thu Jun 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099392 (VAI Mon Aug 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 915677 (NAI Thu Feb 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859946 (NAI Mon Dec 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 754608 (VAI Mon Nov 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources