FDA Inspection 1260405 — Versiti Michigan, Inc.

Versiti Michigan, Inc. — FEI 3005966419

The FDA completed an inspection of Versiti Michigan, Inc. on January 17, 2025 in Grandville, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 17, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grandville, MI (United States)