FDA Inspection 1245903 — Versiti Michigan Inc

Versiti Michigan Inc — FEI 1875548

The FDA completed an inspection of Versiti Michigan Inc on Jun 27, 2024 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
Jun 27, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Grand Rapids, MI (United States)

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