FDA Inspection 900873 — AbbVie Deutschland GmbH & Co. KG

AbbVie Deutschland GmbH & Co. KG — FEI 3002807401

The FDA completed an inspection of AbbVie Deutschland GmbH & Co. KG on September 18, 2014 in Ludwigshafen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ludwigshafen (Germany)