FDA inspection

Genentech Inc: FDA inspection ending Feb 12, 2007

FDA inspection 466243 · No Action Indicated (NAI) · Oceanside, CA

Key facts

Inspection ID 466243
Firm Genentech Inc
FEI number 3006129086
Address 1 Antibody Way
City Oceanside
State CA
ZIP 92056-5701
Fiscal year 2007
Inspection end date Feb 12, 2007
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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