FDA Inspection 548334 — Abbott Laboratories GmbH

Abbott Laboratories GmbH — FEI 3002808216

The FDA completed an inspection of Abbott Laboratories GmbH on Oct 14, 2008 in Neustadt am Rubenberge. 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
Oct 14, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neustadt am Rubenberge (Germany)

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