FDA Inspection 1113802 — Stingray Surgical Products, LLC

Stingray Surgical Products, LLC — FEI 3006059917

The FDA completed an inspection of Stingray Surgical Products, LLC on December 20, 2019 in Boca Raton, FL. 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
December 20, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Boca Raton, FL (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation