FDA Inspection 1010702 — Versiti Michigan, Inc
The FDA completed an inspection of Versiti Michigan, Inc on Apr 5, 2017 in Traverse City, 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
- Apr 5, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Traverse City, MI (United States)