FDA Inspection 649725 — Peter S Fail MD

Peter S Fail MD — FEI 3007969426

The FDA completed an inspection of Peter S Fail MD on Feb 26, 2010 in Houma, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 26, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Houma, LA (United States)

Additional Details

Clinical Investigator (CI)