FDA Inspection 1259220 — Acuity Surgical Devices, LLC

Acuity Surgical Devices, LLC — FEI 3010866843

The FDA completed an inspection of Acuity Surgical Devices, LLC on January 27, 2025 in Irving, TX. 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 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Irving, TX (United States)

Citations

IDCFRDescription
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
235021 CFR 820.25(b)Training - Lack of or inadequate procedures