FDA Inspection 947100 — Interpharma Praha A.S.

Interpharma Praha A.S. — FEI 3002807299

The FDA completed an inspection of Interpharma Praha A.S. on October 16, 2015 in Prague 12. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 16, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Prague 12 (Czech Republic)