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FDA Inspection
•Genentech, Inc.•December 6, 2011

Genentech, Inc. – FDA Inspection, Dec 6, 2011

Record Details

This FDA Inspection record concerns Genentech, Inc., with an inspection on December 6, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Genentech, Inc.
Inspection Date
December 6, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · e8b558cd-60e7-4984-8884-0569dd756ffa

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
759952
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 312.50Ensuring compliance with plan and protocol

Full citation text and observation details available on the Dashboard.

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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