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FDA Inspection
•Genentech, Inc.•July 12, 2017

Genentech, Inc. – FDA Inspection, Jul 12, 2017

Record Details

This FDA Inspection record concerns Genentech, Inc., with an inspection on July 12, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Genentech, Inc.
Inspection Date
July 12, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Stuart W. Russell (FDA Associated Person)
View Company Profile

ID · 73105775-104e-49e4-a9ed-8b8b3c695e86

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1024250
FDA center
Human Drugs
Project area
Bioresearch Monitoring

Other FDA inspections of Genentech, Inc.

34
DateClassificationOfficeProject area
August 4, 2026Not classifiedSan Francisco District Office
May 15, 2026Not classifiedSan Francisco District Office
April 7, 2026Not classifiedSan Francisco District Office
April 21, 2025NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
May 2, 2024VAICenter for Drug Evaluation and ResearchPostmarket Surv. and Epidemiology
View all 34 other inspections on the company page
Other documents for Genentech, Inc.
  • FDA Inspection 1332732 - 2026-08-04
  • FDA Inspection 1322404 - 2026-05-15
  • FDA Inspection 1314654 - 2026-04-07
  • FDA Inspection 1263573 - 2025-04-21
  • FDA Inspection 1236964 - 2024-05-02

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