FDA Inspection 669887 — Stephenson, P. Dee G., Md

Stephenson, P. Dee G., Md — FEI 3008367583

The FDA completed an inspection of Stephenson, P. Dee G., Md on Jun 24, 2010 in Venice, 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 24, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Venice, FL (United States)

Additional Details

Clinical Investigator (CI)