FDA Inspection 1237474 — Creo Medical LTD

Creo Medical LTD — FEI 3014925413

The FDA completed an inspection of Creo Medical LTD on May 2, 2024 in Chepstow. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 2, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Chepstow (United Kingdom)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
73121 CFR 803.50(a)(1)Report of Death or Serious Injury