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FDA Inspection 1037184 — Joseph Biggio, MD

Joseph Biggio, MD — FEI 3013921985

The FDA completed an inspection of Joseph Biggio, MD on Dec 15, 2017 in Birmingham, AL. 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
Dec 15, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Birmingham, AL (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources