FDA inspection

Genentech, Inc.: FDA inspection ending Jul 1, 2014

FDA inspection 888022 · No Action Indicated (NAI) · Hillsboro, OR

Key facts

Inspection ID 888022
Firm Genentech, Inc.
FEI number 3007232634
Address 4625 Ne Brookwood Pkwy
City Hillsboro
State OR
ZIP 97124
Country United States
Fiscal year 2014
Inspection end date Jul 1, 2014
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
  • 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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