FDA Inspection 1266879 — VQ Orthocare

VQ Orthocare — FEI 3002757749

The FDA completed an inspection of VQ Orthocare on Mar 11, 2025 in Vista, CA. 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
Mar 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Vista, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.