FDA Inspection 960098 — Octapharma Dessau GmbH

Octapharma Dessau GmbH — FEI 3008923644

The FDA completed an inspection of Octapharma Dessau GmbH on Feb 18, 2016 in Dessau-Roslau. 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
Feb 18, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dessau-Roslau (Germany)

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