FDA Inspection 770439 — Abbott GmbH

Abbott GmbH — FEI 3002809144

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

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Wiesbaden (Germany)

Additional Details

Postmarket Audit Inspections