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FDA Inspection 969863 — Simtra US LLC

Simtra US LLC — FEI 1000115571

The FDA completed an inspection of Simtra US LLC on May 12, 2016 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
May 12, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bloomington, IN (United States)

Facility

Other inspections at this facility

  • 1242468 (VAI Tue Sep 24 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1200813 (NAI Fri Feb 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1157719 (VAI Wed Nov 10 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060004 (VAI Wed May 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1019766 (VAI Mon Jul 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources