FDA Inspection 847776 — Versiti Michigan, Inc.

Versiti Michigan, Inc. — FEI 3005966419

The FDA completed an inspection of Versiti Michigan, Inc. on Sep 5, 2013 in Grandville, 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 5, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grandville, MI (United States)

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