FDA Inspection 1171878 — Rigicon, Inc.

Rigicon, Inc. — FEI 3013987875

The FDA completed an inspection of Rigicon, Inc. on Jun 8, 2022 in Ronkonkoma, NY. 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
Jun 8, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Ronkonkoma, NY (United States)