FDA Inspection 1101493 — Vitalant

Vitalant — FEI 2976506

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.