FDA Inspection 1332402 — OrthoGrid System, Inc.
The FDA completed an inspection of OrthoGrid System, Inc. on Aug 7, 2026 in Midvale, UT. 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 7, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Midvale, UT (United States)