FDA Inspection 817877 — IDT Biologika GmbH

IDT Biologika GmbH — FEI 3005001757

The FDA completed an inspection of IDT Biologika GmbH on October 18, 2012 in Dessau-Rosslau. 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
October 18, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dessau-Rosslau (Germany)