FDA Inspection 1335226 — Craniomandibular Rehab Inc

Craniomandibular Rehab Inc — FEI 3000215572

The FDA completed an inspection of Craniomandibular Rehab Inc on Sep 9, 2026 in Wheat Ridge, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 9, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wheat Ridge, CO (United States)