FDA Inspection 1236134 — Maxx Ortopedics Inc

Maxx Ortopedics Inc — FEI 3007311878

The FDA completed an inspection of Maxx Ortopedics Inc on May 16, 2025 in West Norriton, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
West Norriton, PA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation