FDA inspection

Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc.: FDA inspection ending Jul 10, 2009

FDA inspection 596461 · No Action Indicated (NAI) · Rouses Point, NY

Key facts

Inspection ID 596461
Firm Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc.
FEI number 1310337
Address 64 Maple St
City Rouses Point
State NY
ZIP 12979
Country United States
Fiscal year 2009
Inspection end date Jul 10, 2009
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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