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 April 4, 2017 in Fegersheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 4, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fegersheim (France)