FDA Inspection 647642 — Czech-Gen, A.S.

Czech-Gen, A.S. — FEI 3002806982

The FDA completed an inspection of Czech-Gen, A.S. on Feb 19, 2010 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
Feb 19, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Olomouc (Czech Republic)