FDA Inspection 1308006 — Renishaw Neuro Solutions Ltd.

Renishaw Neuro Solutions Ltd. — FEI 3017004815

The FDA completed an inspection of Renishaw Neuro Solutions Ltd. on March 19, 2026 in Wotton-Under-Edge. 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
March 19, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Wotton-Under-Edge (United Kingdom)

Citations

IDCFRDescription
23255ISO 13485:2016 Clause 8.5.2Corrective action not taken