FDA Inspection 1278899 — UIH Technologies LLC

UIH Technologies LLC — FEI 3014809646

The FDA completed an inspection of UIH Technologies LLC on Aug 20, 2025 in Houston, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 20, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
2279621 CFR 801.40(a)Form of a unique device identifier
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures

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