FDA Inspection 833163 — 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 May 22, 2013 in Prague 9. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 22, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Prague 9 (Czech Republic)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.