FDA Inspection 1054865 — Arkema Inc

Arkema Inc — FEI 1020326

The FDA completed an inspection of Arkema Inc on Jun 7, 2018 in Memphis, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 7, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Memphis, TN (United States)

Citations

IDCFRDescription
440421 CFR 211.194(a)(1)Sample identification and other information