FDA Inspection 1063852 — LifeStream Blood Bank

LifeStream Blood Bank — FEI 2074143

The FDA completed an inspection of LifeStream Blood Bank on Aug 23, 2018 in San Bernardino, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 23, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Bernardino, CA (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report

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