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FDA Inspection 802518 — Versiti Wisconsin, Inc.

Versiti Wisconsin, Inc. — FEI 3002930204

The FDA completed an inspection of Versiti Wisconsin, Inc. on October 2, 2012 in Milwaukee, WI. 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 2, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Milwaukee, WI (United States)

Facility

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  • 1114817 (NAI Fri Dec 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1035583 (NAI Mon Dec 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946198 (NAI Wed Sep 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 763579 (NAI Thu Jan 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources