FDA Inspection 1287472 — ZMICRO, INC.

ZMICRO, INC. — FEI 3008142630

The FDA completed an inspection of ZMICRO, INC. on Oct 16, 2025 in San Diego, CA. 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
Oct 16, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
2280121 CFR 830.310(b)GUDID Information required for unique device identification.

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