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FDA Inspection 713864 — Esteve CDMO US, Inc.

Esteve CDMO US, Inc. — FEI 1416120

The FDA completed an inspection of Esteve CDMO US, Inc. on March 8, 2011 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
March 8, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morton Grove, IL (United States)

Facility

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