FDA Inspection 1058044 — Azenta Life Sciences, Inc

Azenta Life Sciences, Inc — FEI 3004757032

The FDA completed an inspection of Azenta Life Sciences, Inc on July 6, 2018 in Indianapolis, IN. 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
July 6, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Indianapolis, IN (United States)

Citations

IDCFRDescription
1237121 CFR 1271.200(a)Cleaned, sanitized per established schedules