FDA Inspection 933280 — UAB Teva Baltics

UAB Teva Baltics — FEI 3008110727

The FDA completed an inspection of UAB Teva Baltics on July 3, 2015 in Vilnius. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 3, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vilnius (Lithuania)