FDA inspection

Genentech, Inc.: FDA inspection ending May 21, 2021

FDA inspection 1142478 · Voluntary Action Indicated (VAI) · Hillsboro, OR

Key facts

Inspection ID 1142478
Firm Genentech, Inc.
FEI number 3007232634
Address 4625 Ne Brookwood Pkwy
City Hillsboro
State OR
ZIP 97124-5301
Fiscal year 2021
Inspection end date May 21, 2021
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
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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