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 Jun 5, 2009 in Prague 9. 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 5, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Prague 9 (Czech Republic)

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