FDA Inspection 1004228 — Wacker Leon SL.

Wacker Leon SL. — FEI 3002806372

The FDA completed an inspection of Wacker Leon SL. on Jan 20, 2017 in Leon. 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
Jan 20, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leon (Spain)

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