FDA Inspection 793700 — Novo Nordisk A/S - Hax

Novo Nordisk A/S - Hax — FEI 3002807748

The FDA completed an inspection of Novo Nordisk A/S - Hax on Jun 26, 2012 in Gentofte. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 26, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gentofte (Denmark)

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