FDA Inspection 1029554 — Arthur L. Burnett, MD

Arthur L. Burnett, MD — FEI 3013641329

The FDA completed an inspection of Arthur L. Burnett, MD on Oct 2, 2017 in Baltimore, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 2, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Sponsor-Investigator (S-I)