FDA Inspection 933821 — Versiti Michigan, Inc.
The FDA completed an inspection of Versiti Michigan, Inc. on Jul 10, 2015 in Grandville, MI. 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
- Jul 10, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Grandville, MI (United States)