FDA Inspection 1101493 — Vitalant

Vitalant — FEI 2976506

The FDA completed an inspection of Vitalant on September 4, 2019 in San Francisco, 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
September 4, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Francisco, CA (United States)