FDA Inspection 1192276 — Octapharma S.A.S.

Octapharma S.A.S. — FEI 3010600159

The FDA completed an inspection of Octapharma S.A.S. on Dec 6, 2022 in Lingolsheim. 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: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 6, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lingolsheim (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.