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FDA Inspection
•Exelixis, Inc.•May 5, 2026

Exelixis, Inc. – FDA Inspection, May 5, 2026

Record Details

This FDA Inspection record concerns Exelixis, Inc., with an inspection on May 5, 2026, issued by the San Francisco District Office, covering human drugs.

Company
Exelixis, Inc.
Inspection Date
May 5, 2026
Product Type
Human Drugs
Office
San Francisco District Office
Person
  • Cynthia J. Tsui (Investigator)
View Company Profile

ID · d1b3bb11-6beb-4455-89a0-921c99e321ad

Inspection Facts

Inspection number
1319178
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 312.50General responsibilities of sponsors

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Exelixis, Inc.

2
DateClassificationOfficeProject area
March 27, 2018NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
September 27, 2012OAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Exelixis, Inc.
  • FDA Inspection 1049904 - 2018-03-27
  • FDA Inspection 802660 - 2012-09-27

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