FDA Inspection 1255908 — Immunexpress, Inc

Immunexpress, Inc — FEI 3016504919

The FDA completed an inspection of Immunexpress, Inc on Dec 6, 2024 in Seattle, WA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 6, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Seattle, WA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures

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