FDA Inspection 800205 — Michael J Biunno, MD

Michael J Biunno, MD — FEI 3009560631

The FDA completed an inspection of Michael J Biunno, MD on Sep 20, 2012 in New Orleans, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 20, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New Orleans, LA (United States)

Additional Details

Clinical Investigator (CI)