FDA Inspection 1055095 — Debiopharm Research & Manufacturing S.A.

Debiopharm Research & Manufacturing S.A. — FEI 3002806850

The FDA completed an inspection of Debiopharm Research & Manufacturing S.A. on June 8, 2018 in Martigny. 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
Martigny (Switzerland)

Citations

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