FDA Inspection 548022 — Vitalant

Vitalant — FEI 3000717965

The FDA completed an inspection of Vitalant on November 20, 2008 in Canton, OH. 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
November 20, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Canton, OH (United States)