FDA Inspection 1151683 — Regulus Global

Regulus Global — FEI 3009802091

The FDA completed an inspection of Regulus Global on July 30, 2021 in Virginia Beach, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 30, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Virginia Beach, VA (United States)