FDA Inspection 1298612 — Apex Medical Technologies, Inc.

Apex Medical Technologies, Inc. — FEI 2025773

The FDA completed an inspection of Apex Medical Technologies, Inc. on January 15, 2026 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 15, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures