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FDA Inspection 933821 — Versiti Michigan, Inc.

Versiti Michigan, Inc. — FEI 3005966419

The FDA completed an inspection of Versiti Michigan, Inc. on July 10, 2015 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
July 10, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grandville, MI (United States)

Facility

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FDA data resources