FDA Inspection 1099221 — Vitalant

Vitalant — FEI 2970618

The FDA completed an inspection of Vitalant on August 6, 2019 in San Mateo, 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
August 6, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Mateo, CA (United States)