FDA Inspection 1020179 — CamNtech Ltd

CamNtech Ltd — FEI 3007485597

The FDA completed an inspection of CamNtech Ltd on August 3, 2017 in Cambridgeshire. 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
August 3, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Cambridgeshire (United Kingdom)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures