FDA Inspection 810800 — Arkema Inc

Arkema Inc — FEI 1020326

The FDA completed an inspection of Arkema Inc on Dec 12, 2012 in Memphis, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 12, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Memphis, TN (United States)