FDA Inspection 814196 — Czech-Gen, A.S.

Czech-Gen, A.S. — FEI 3002806982

The FDA completed an inspection of Czech-Gen, A.S. on Dec 14, 2012 in Olomouc. 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
Dec 14, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Olomouc (Czech Republic)