FDA Inspection 913113 — Patrick Aiello

Patrick Aiello — FEI 3007898018

The FDA completed an inspection of Patrick Aiello on Jan 29, 2015 in Yuma, AZ. 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
Jan 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Yuma, AZ (United States)

Additional Details

Clinical Investigator (CI)