FDA Inspection 875285 — Pierce D Nunley MD

Pierce D Nunley MD — FEI 3007198735

The FDA completed an inspection of Pierce D Nunley MD on Feb 28, 2014 in Shreveport, 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 28, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Shreveport, LA (United States)

Additional Details

Clinical Investigator (CI)