FDA inspection

Genentech, Inc.: FDA inspection ending Jun 27, 2012

FDA inspection 791162 · Voluntary Action Indicated (VAI) · Hillsboro, OR

Key facts

Inspection ID 791162
Firm Genentech, Inc.
FEI number 3007232634
Address 4625 Ne Brookwood Pkwy
City Hillsboro
State OR
ZIP 97124
Country United States
Fiscal year 2012
Inspection end date Jun 27, 2012
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
  • Yes 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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