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FDA Inspection
•Astellas Pharma Inc.•November 7, 2008

Astellas Pharma Inc. – FDA Inspection, Nov 7, 2008

Record Details

This FDA Inspection record concerns Astellas Pharma Inc., with an inspection on November 7, 2008, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Astellas Pharma Inc.
Inspection Date
November 7, 2008
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · f2647247-4f2e-4543-b111-52cad2d1e7e2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
548559
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Astellas Pharma Inc.

5
DateClassificationOfficeProject area
June 6, 2025VAIOffice of Inspections and InvestigationsDrug Quality Assurance
March 5, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 18, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 11, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 21, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Astellas Pharma Inc.
  • FDA Inspection 1274944 - 2025-06-06
  • FDA Inspection 1081668 - 2019-03-05
  • FDA Inspection 963371 - 2016-03-18
  • FDA Inspection 874760 - 2014-04-11
  • FDA Inspection 756552 - 2011-11-21

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