FDA Inspection 1157719 — Simtra US LLC

Simtra US LLC — FEI 1000115571

The FDA completed an inspection of Simtra US LLC on November 10, 2021 in Bloomington, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 10, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Bloomington, IN (United States)