FDA Inspection 1180282 — Rampart IC LLC

Rampart IC LLC — FEI 3016257387

The FDA completed an inspection of Rampart IC LLC on Aug 16, 2022 in Vestavia, AL. 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
Aug 16, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Vestavia, AL (United States)