FDA Inspection 770439 — Abbott GmbH

Abbott GmbH — FEI 3002809144

The FDA completed an inspection of Abbott GmbH on Feb 9, 2012 in Wiesbaden. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wiesbaden (Germany)

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