FDA inspection

Genentech, Inc.: FDA inspection ending Aug 11, 2023

FDA inspection 1214575 · Voluntary Action Indicated (VAI) · South San Francisco, CA

Key facts

Inspection ID 1214575
Firm Genentech, Inc.
FEI number 2917293
Address 1 Dna Way Ms 40-8
City South San Francisco
State CA
ZIP 94080
Country United States
Fiscal year 2023
Inspection end date Aug 11, 2023
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • 1–9 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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