FDA inspection

Genentech Inc: FDA inspection ending Aug 26, 2016

FDA inspection 985946 · Voluntary Action Indicated (VAI) · Vacaville, CA

Key facts

Inspection ID 985946
Firm Genentech Inc
FEI number 3002902534
Address 1000 New Horizons Way
City Vacaville
State CA
ZIP 95688-9431
Fiscal year 2016
Inspection end date Aug 26, 2016
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
  • 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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