FDA Inspection 825126 — Barbara A. Burtner

Barbara A. Burtner — FEI 3009956896

The FDA completed an inspection of Barbara A. Burtner on Mar 20, 2013 in Kissimmee, FL. 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
Mar 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kissimmee, FL (United States)

Additional Details

Clinical Investigator (CI)