FDA Inspection 1204393 — Kathleen M. Mullane, D.O.

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

The FDA completed an inspection of Kathleen M. Mullane, D.O. on April 28, 2023 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 28, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)