FDA Inspection
Codan US CorporationCodan US Corporation – FDA Inspection, Jul 20, 2018
Record Details
This FDA Inspection record concerns Codan US Corporation, with an inspection on July 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ac5ea224-cd5e-4661-8972-80afc07d5213
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059719
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of Codan US Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 18, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 16, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Codan US Corporation
- FDA Inspection 883590 - 2014-06-18
- FDA Inspection 612137 - 2009-09-16
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