FDA Inspection 1217677 — Immersivetouch Inc

Immersivetouch Inc — FEI 3014833795

The FDA completed an inspection of Immersivetouch Inc on Sep 14, 2023 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 14, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
341521 CFR 820.22Quality Audit/Reaudit - conducted

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