FDA Inspection 999212 — Versiti Wisconsin, Inc.
The FDA completed an inspection of Versiti Wisconsin, Inc. on Nov 1, 2016 in West Bend, 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
- Nov 1, 2016
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- West Bend, WI (United States)