FDA Inspection 1059719 — Codan US Corporation

Codan US Corporation — FEI 2016945

The FDA completed an inspection of Codan US Corporation on Jul 20, 2018 in Santa Ana, CA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Ana, CA (United States)

Citations

IDCFRDescription
320721 CFR 820.50(b)Supplier notification of changes