FDA Inspection 1257699 — Konapharma AG

Konapharma AG — FEI 3002996751

The FDA completed an inspection of Konapharma AG on Jun 19, 2024 in Pratteln. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pratteln (Switzerland)

Additional Details

Mutual Recognition Agreement (MRA)