FDA Inspection 1125458 — Kathleen M. Mullane, D.O.

Kathleen M. Mullane, D.O. — FEI 3008706262

The FDA completed an inspection of Kathleen M. Mullane, D.O. on July 20, 2020 in Chicago, IL. 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
July 20, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)