FDA Inspection 1217677 — Immersivetouch Inc

Immersivetouch Inc — FEI 3014833795

The FDA completed an inspection of Immersivetouch Inc on September 14, 2023 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 14, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: 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