FDA inspection

Genentech, Inc.: FDA inspection ending Sep 26, 2011

FDA inspection 746619 · Voluntary Action Indicated (VAI) · South San Francisco, CA

Key facts

Inspection ID 746619
Firm Genentech, Inc.
FEI number 2917293
Address 1 Dna Way
City South San Francisco
State CA
ZIP 94080
Country United States
Fiscal year 2011
Inspection end date Sep 26, 2011
Classification Voluntary Action Indicated (VAI)
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
  • 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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