FDA Inspection 1047502 — Magdalena Wieczorek-Rutkowska M.D.

Magdalena Wieczorek-Rutkowska M.D. — FEI 3013850045

The FDA completed an inspection of Magdalena Wieczorek-Rutkowska M.D. on Jan 19, 2018 in Gdansk. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 19, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Gdansk (Poland)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.