FDA Inspection 1102761 — Iwona Kobielusz-Gembala

Iwona Kobielusz-Gembala — FEI 3014932053

The FDA completed an inspection of Iwona Kobielusz-Gembala on March 15, 2019 in Oswiecim. 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 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Oswiecim (Poland)

Additional Details

Clinical Investigator (CI)