Home / Inspections / 991585

FDA Inspection 991585 — Catalent Indiana, LLC

Catalent Indiana, LLC — FEI 3005949964

The FDA completed an inspection of Catalent Indiana, LLC on August 24, 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
August 24, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bloomington, IN (United States)

Facility

Other inspections at this facility

  • 1264264 (OAI Mon Jul 14 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1224264 (VAI Wed Nov 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1178819 (VAI Thu Sep 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111350 (VAI Fri Oct 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1063669 (NAI Fri Aug 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources