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FDA Inspection
•Epax Norway AS•September 22, 2017

Epax Norway AS – FDA Inspection, Sep 22, 2017

Record Details

This FDA Inspection record concerns Epax Norway AS, with an inspection on September 22, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Epax Norway AS
Inspection Date
September 22, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Helen B. Ricalde (FDA Associated Person)
View Company Profile

ID · 8fe600e7-7c43-4ff6-b4c0-7b4293f39d4f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1029746
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Epax Norway AS

1
DateClassificationOfficeProject area
October 10, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Epax Norway AS
  • FDA Inspection 854875 - 2013-10-10

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