FDA Inspection 751962 — Mary Petruso

Mary Petruso — FEI 3009214596

The FDA completed an inspection of Mary Petruso on Oct 31, 2011 in Fort Lauderdale, FL. 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
Oct 31, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fort Lauderdale, FL (United States)

Additional Details

Clinical Investigator (CI)