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FDA Inspection
•ID Biomedical Corporation of Quebec•May 26, 2017

ID Biomedical Corporation of Quebec – FDA Inspection, May 26, 2017

Record Details

This FDA Inspection record concerns ID Biomedical Corporation of Quebec, with an inspection on May 26, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
ID Biomedical Corporation of Quebec
Inspection Date
May 26, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Burnell M. Henry (FDA Associated Person)
  • Prabhu P. Raju (FDA Associated Person)
View Company Profile

ID · ceb3d4c5-2426-4493-abb8-df1fd01d470b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1012864
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

Other FDA inspections of ID Biomedical Corporation of Quebec

7
DateClassificationOfficeProject area
March 28, 2025Not classifiedOffice of Inspections and Investigations
May 20, 2022VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 5, 2015VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
April 9, 2014OAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
April 7, 2011VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 7 other inspections on the company page
Other documents for ID Biomedical Corporation of Quebec
  • FDA Inspection 1256961 - 2025-03-28
  • FDA Inspection 1171029 - 2022-05-20
  • FDA Inspection 941226 - 2015-06-05
  • FDA Inspection 878510 - 2014-04-09
  • FDA Inspection 723187 - 2011-04-07

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