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FDA Inspection 804580 — Lisa Brailey, MD

Lisa Brailey, MD — FEI 3009728675

The FDA completed an inspection of Lisa Brailey, MD on Oct 24, 2012 in Shelton, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 24, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Shelton, CT (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources