FDA inspection

Advent Pharmaceuticals Inc.: FDA inspection ending Aug 10, 2001

FDA inspection 85200 · Official Action Indicated (OAI) · Hightstown, NJ

Key facts

Inspection ID 85200
Firm Advent Pharmaceuticals Inc.
FEI number 1000136032
Address 55 Lake Dr
City Hightstown
State NJ
ZIP 08520-5320
Fiscal year 2001
Inspection end date Aug 10, 2001
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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