FDA Inspection 1288394 — Koya Medical, Inc

Koya Medical, Inc — FEI 3033981998

The FDA completed an inspection of Koya Medical, Inc on Oct 24, 2025 in Dallas, TX. 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 24, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)

Citations

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

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