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FDA Inspection
•SmartPractice Denmark ApS•April 5, 2019

SmartPractice Denmark ApS – FDA Inspection, Apr 5, 2019

Record Details

This FDA Inspection record concerns SmartPractice Denmark ApS, with an inspection on April 5, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
SmartPractice Denmark ApS
Inspection Date
April 5, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Debra M. Emerson (FDA Associated Person)
View Company Profile

ID · e1573c1d-f572-40fb-849d-abdead2f8c71

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1090369
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

Other FDA inspections of SmartPractice Denmark ApS

5
DateClassificationOfficeProject area
August 16, 2024NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
January 29, 2016VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
January 28, 2014VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 11, 2011VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 17, 2009VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
Other documents for SmartPractice Denmark ApS
  • FDA Inspection 1253548 - 2024-08-16
  • FDA Inspection 962561 - 2016-01-29
  • FDA Inspection 879358 - 2014-01-28
  • FDA Inspection 757164 - 2011-11-11
  • FDA Inspection 620002 - 2009-09-17

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