FDA Inspection 706188 — Pacheco Sixto

Pacheco Sixto — FEI 3008685743

The FDA completed an inspection of Pacheco Sixto on Dec 8, 2010 in Miami, 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
Dec 8, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)