FDA Inspection 759148 — Vitalant

Vitalant — FEI 2077785

The FDA completed an inspection of Vitalant on Dec 14, 2011 in Santa Maria, CA. 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
Dec 14, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Maria, CA (United States)

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