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FDA Inspection 981668 — Esteve CDMO US, Inc.

Esteve CDMO US, Inc. — FEI 1416120

The FDA completed an inspection of Esteve CDMO US, Inc. on August 15, 2016 in Morton Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morton Grove, IL (United States)

Facility

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  • 1091835 (NAI Tue Apr 23 2019 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