FDA Inspection 1052699 — Duckworth & Kent, Ltd.

Duckworth & Kent, Ltd. — FEI 1000231766

The FDA completed an inspection of Duckworth & Kent, Ltd. on May 17, 2018 in Baldock. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Baldock (United Kingdom)