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FDA Inspection 583267 — Esteve CDMO US, Inc.

Esteve CDMO US, Inc. — FEI 1416120

The FDA completed an inspection of Esteve CDMO US, Inc. on May 8, 2009 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 8, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Morton Grove, IL (United States)

Additional Details

Postmarket Audit Inspections

Facility

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FDA data resources