FDA Inspection 1027893 — Shiseido International France S.A.S.

Shiseido International France S.A.S. — FEI 1000572066

The FDA completed an inspection of Shiseido International France S.A.S. on July 25, 2017 in Gien. 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
July 25, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gien (France)