FDA Inspection 1107966 — Abbott Laboratories GmbH

Abbott Laboratories GmbH — FEI 3002808216

The FDA completed an inspection of Abbott Laboratories GmbH on Aug 30, 2019 in Neustadt am Rubenberge. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 30, 2019
Fiscal Year
2019
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.