FDA Inspection 573491 — Versiti Wisconsin, Inc
The FDA completed an inspection of Versiti Wisconsin, Inc on Mar 25, 2009 in Waukesha, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 25, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Waukesha, WI (United States)