FDA Inspection 1055111 — Patheon France S.A.S.

Patheon France S.A.S. — FEI 3004468553

The FDA completed an inspection of Patheon France S.A.S. on June 8, 2018 in Bourgoin Jallieu Cedex. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 8, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bourgoin Jallieu Cedex (France)

Citations

IDCFRDescription
145021 CFR 211.113(a)Procedures for non-sterile drug products