FDA Inspection 1178635 — Uscom Limited

Uscom Limited — FEI 3004987887

The FDA completed an inspection of Uscom Limited on Sep 1, 2022 in Sydney. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 1, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Sydney (Australia)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
334521 CFR 820.200(a)Servicing - Lack of or inadequate procedures

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