FDA Inspection 941875 — Vitalant

Vitalant — FEI 2970030

The FDA completed an inspection of Vitalant on Sep 11, 2015 in Yuba City, 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
Sep 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuba City, CA (United States)

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