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FDA Inspection 1264016 — Versiti Indiana, Inc.

Versiti Indiana, Inc. — FEI 1828129

The FDA completed an inspection of Versiti Indiana, Inc. on March 11, 2025 in Lafayette, IN. 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
March 11, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, IN (United States)

Facility

Other inspections at this facility

  • 1214844 (NAI Fri Aug 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032128 (NAI Wed Nov 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 957611 (NAI Tue Feb 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884440 (NAI Tue Jun 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 799301 (VAI Tue Sep 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources