FDA Inspection 1040771 — Alvelogro Inc

Alvelogro Inc — FEI 3006558294

The FDA completed an inspection of Alvelogro Inc on February 12, 2018 in Snoqualmie, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 12, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Snoqualmie, WA (United States)

Citations

IDCFRDescription
1241621 CFR 1271.260(e)Storage temperatures recorded, maintained