FDA Inspection 1298386 — AVATION MEDICAL

AVATION MEDICAL — FEI 3027578962

The FDA completed an inspection of AVATION MEDICAL on Dec 11, 2025 in Columbus, OH. 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 11, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (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.