FDA Inspection 1070209 — Rigicon, Inc.
The FDA completed an inspection of Rigicon, Inc. on Oct 19, 2018 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
- Oct 19, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Ronkonkoma, NY (United States)