FDA Inspection 1031211 — Evonik Operations GmbH

Evonik Operations GmbH — FEI 3002808332

The FDA completed an inspection of Evonik Operations GmbH on Sep 29, 2017 in Dossenheim. 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
Sep 29, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dossenheim (Germany)

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