FDA Inspection 984997 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on Sep 15, 2016 in Grand Rapids, 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
Sep 15, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Rapids, MI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.