FDA Inspection 583012 — Advent Pharmaceuticals Inc.

Advent Pharmaceuticals Inc. — FEI 1000136032

The FDA completed an inspection of Advent Pharmaceuticals Inc. on Apr 30, 2009 in Hightstown, NJ. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Apr 30, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hightstown, NJ (United States)

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