FDA Inspection 1017658 — Abbott Laboratories GmbH

Abbott Laboratories GmbH — FEI 3002808216

The FDA completed an inspection of Abbott Laboratories GmbH on Feb 24, 2017 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
Feb 24, 2017
Fiscal Year
2017
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.