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FDA Inspection
•Eisai, Inc.•September 15, 2026

Eisai, Inc. – FDA Inspection, Sep 15, 2026

Record Details

This FDA Inspection record concerns Eisai, Inc., with an inspection on September 15, 2026, issued by the Baltimore District Office, covering human drugs.

Company
Eisai, Inc.
Inspection Date
September 15, 2026
Product Type
Human Drugs
Office
Baltimore District Office
People
  • Claude Noel Y. Zanetsie (Issuing Officer)
  • Daniel L. Zheng (FDA Associated Person)
View Company Profile

ID · 21cba403-4bda-47f1-b50e-b846dfd35feb

Inspection Facts

Inspection number
1335274
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Eisai, Inc.

5
DateClassificationOfficeProject area
April 9, 2024VAICenter for Drug Evaluation and ResearchNew Drug Evaluation
July 22, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 17, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 9, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 12, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eisai, Inc.
  • FDA Inspection 1237510 - 2024-04-09
  • FDA Inspection 977950 - 2016-07-22
  • FDA Inspection 860646 - 2013-12-17
  • FDA Inspection 722050 - 2011-05-09
  • FDA Inspection 669338 - 2010-05-12

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