FDA Inspection 1053176 — Anatol Mickielewicz, M.D.

Anatol Mickielewicz, M.D. — FEI 3014240250

The FDA completed an inspection of Anatol Mickielewicz, M.D. on May 10, 2018 in Warsaw. 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
May 10, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Warsaw (Poland)

Additional Details

Clinical Investigator (CI)