FDA Inspection 954070 — Eurofarma, Inc.

Eurofarma, Inc. — FEI 3008297643

The FDA completed an inspection of Eurofarma, Inc. on December 7, 2015 in Parsippany, NJ. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 7, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Parsippany, NJ (United States)