FDA Inspection 1155685 — Arkema, Inc.

Arkema, Inc. — FEI 1314624

The FDA completed an inspection of Arkema, Inc. on September 22, 2021 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
September 22, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Piffard, NY (United States)