FDA Inspection 1020863 — Lilly France S.A.S.

Lilly France S.A.S. — FEI 3002807475

The FDA completed an inspection of Lilly France S.A.S. on Apr 4, 2017 in Fegersheim. 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
Apr 4, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fegersheim (France)

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