FDA Inspection 960526 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1876521

The FDA completed an inspection of Versiti Michigan Inc on Jan 25, 2016 in Bay 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
Jan 25, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bay City, MI (United States)

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