FDA Inspection
D E Hokanson IncD E Hokanson Inc – FDA Inspection, Mar 19, 2015
Record Details
This FDA Inspection record concerns D E Hokanson Inc, with an inspection on March 19, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- D E Hokanson Inc
- Inspection Date
- March 19, 2015
- Product Type
- Devices
View Company Profile
ID · ccf4406a-3387-4520-ac24-8c4b87bb5fd7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 918525
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.75(a)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of D E Hokanson Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 7, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 30, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 21, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 8, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for D E Hokanson Inc
- FDA Inspection 1040113 - 2018-02-07
- FDA Inspection 804776 - 2012-10-30
- FDA Inspection 703422 - 2010-12-21
- FDA Inspection 584834 - 2009-05-08
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