FDA Inspection 629512 — William P Coleman, III, MD

William P Coleman, III, MD — FEI 3003778211

The FDA completed an inspection of William P Coleman, III, MD on November 12, 2009 in Metairie, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 12, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Metairie, LA (United States)

Additional Details

Clinical Investigator (CI)