FDA Inspection 1099987 — Wacker Leon SL.

Wacker Leon SL. — FEI 3002806372

The FDA completed an inspection of Wacker Leon SL. on Oct 18, 2018 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
Oct 18, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leon (Spain)

Additional Details

Mutual Recognition Agreement (MRA)

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