FDA Inspection 839385 — Abbott GmbH

Abbott GmbH — FEI 3002809144

The FDA completed an inspection of Abbott GmbH on June 13, 2013 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
June 13, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wiesbaden (Germany)