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FDA Inspection 588256 — Versiti Wisconsin, Inc.

Versiti Wisconsin, Inc. — FEI 3002930204

The FDA completed an inspection of Versiti Wisconsin, Inc. on June 4, 2009 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
June 4, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Milwaukee, WI (United States)

Facility

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