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FDA Inspection
•Genzyme Corporation•October 22, 2010

Genzyme Corporation – FDA Inspection, Oct 22, 2010

Record Details

This FDA Inspection record concerns Genzyme Corporation, with an inspection on October 22, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Genzyme Corporation
Inspection Date
October 22, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 81df17e8-9782-4308-9965-3fc0c82e6140

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
684675
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Genzyme Corporation

8
DateClassificationOfficeProject area
April 9, 2026Not classifiedNew England District Office
July 9, 2024OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 2, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 21, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Genzyme Corporation
  • FDA Inspection 1294652 - 2026-04-09
  • FDA Inspection 1232210 - 2024-07-09
  • FDA Inspection 1176107 - 2022-07-25
  • FDA Inspection 1003362 - 2017-02-02
  • FDA Inspection 904958 - 2014-11-21

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