FDA Inspection 1194258 — Octapharma Pharmazeutika Produktionsgesellschaft M.B.H.

Octapharma Pharmazeutika Produktionsgesellschaft M.B.H. — FEI 3002809097

The FDA completed an inspection of Octapharma Pharmazeutika Produktionsgesellschaft M.B.H. on Dec 16, 2022 in Vienna. 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 16, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vienna (Austria)

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