FDA Inspection 827273 — Konapharma AG

Konapharma AG — FEI 3002996751

The FDA completed an inspection of Konapharma AG on Apr 17, 2013 in Pratteln. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pratteln (Switzerland)