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FDA Inspection 1193468 — Esteve CDMO US, Inc.

Esteve CDMO US, Inc. — FEI 1416120

The FDA completed an inspection of Esteve CDMO US, Inc. on November 16, 2022 in Morton Grove, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 16, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morton Grove, IL (United States)

Facility

Other inspections at this facility

  • 1091835 (NAI Tue Apr 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 981668 (NAI Mon Aug 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 858655 (NAI Tue Dec 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 774859 (NAI Fri Mar 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 713864 (VAI Tue Mar 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources