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FDA Inspection 911614 — Eurofarma, Inc.

Eurofarma, Inc. — FEI 3008297643

The FDA completed an inspection of Eurofarma, Inc. on January 28, 2015 in Parsippany, 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
January 28, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Parsippany, NJ (United States)

Facility

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  • 1066468 (VAI Tue Aug 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 954070 (OAI Mon Dec 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources