FDA Inspection 1041770 — Actavis Elizabeth LLC

Actavis Elizabeth LLC — FEI 2211563

The FDA completed an inspection of Actavis Elizabeth LLC on February 5, 2018 in Elizabeth, NJ. 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
February 5, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Elizabeth, NJ (United States)