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FDA Inspection 728746 — Arkema, Inc.

Arkema, Inc. — FEI 1314624

The FDA completed an inspection of Arkema, Inc. on May 23, 2011 in Piffard, NY. 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
May 23, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Piffard, NY (United States)

Facility

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