FDA Inspection 590376 — ALS Czech Republic, S.R.O.

ALS Czech Republic, S.R.O. — FEI 3006712025

The FDA completed an inspection of ALS Czech Republic, S.R.O. on June 5, 2009 in Prague 9. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 5, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Prague 9 (Czech Republic)