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FDA Inspection
•Przedsiebiorstwo Farmaceutyczne Jelfa SA•October 22, 2010

Przedsiebiorstwo Farmaceutyczne Jelfa SA – FDA Inspection, Oct 22, 2010

Record Details

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

Company
Przedsiebiorstwo Farmaceutyczne Jelfa SA
Inspection Date
October 22, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 14f49b07-15e1-4ac8-8318-6be021e6f893

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
700751
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Przedsiebiorstwo Farmaceutyczne Jelfa SA

5
DateClassificationOfficeProject area
November 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 13, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 22, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 15, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Przedsiebiorstwo Farmaceutyczne Jelfa SA
  • FDA Inspection 1217692 - 2022-11-25
  • FDA Inspection 1050200 - 2018-03-13
  • FDA Inspection 991418 - 2016-09-22
  • FDA Inspection 885404 - 2014-06-30
  • FDA Inspection 794037 - 2012-05-15

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