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FDA Inspection 1050200 — Przedsiebiorstwo Farmaceutyczne Jelfa SA

Przedsiebiorstwo Farmaceutyczne Jelfa SA — FEI 3004680543

The FDA completed an inspection of Przedsiebiorstwo Farmaceutyczne Jelfa SA on March 13, 2018 in Jelenia Gora. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 13, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jelenia Gora (Poland)

Facility

Other inspections at this facility

  • 1217692 (VAI Fri Nov 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 991418 (VAI Thu Sep 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885404 (NAI Mon Jun 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 794037 (VAI Tue May 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 700751 (OAI Fri Oct 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources