FDA Inspection 1063207 — Evonik Corporation

Evonik Corporation — FEI 3012757951

The FDA completed an inspection of Evonik Corporation on Aug 10, 2018 in Birmingham, AL. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 10, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Birmingham, AL (United States)