FDA Inspection 1095038 — Vitalant

Vitalant — FEI 2976180

The FDA completed an inspection of Vitalant on June 12, 2019 in Chico, CA. 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
June 12, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chico, CA (United States)