FDA Inspection 1181602 — PREMIER NORTH AMERICA

PREMIER NORTH AMERICA — FEI 3014412531

The FDA completed an inspection of PREMIER NORTH AMERICA on Jul 28, 2022 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
Jul 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fort Lauderdale, FL (United States)