# D E Hokanson Inc – FDA Inspection, Feb 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/d-e-hokanson-inc/e924555d-8e4f-4689-b03f-5e60c5eeb986
Source feed: FDA_Inspections

> FDA inspection 1040113 of D E Hokanson Inc, February 07, 2018. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040113
- Company Name: D E Hokanson Inc
- Inspection Date: 2018-02-07
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 918525 - 2015-03-19](https://www.keypedia.com/records/fda_inspections/d-e-hokanson-inc/ccf4406a-3387-4520-ac24-8c4b87bb5fd7)
- FDA Inspection 804776 - 2012-10-30
- FDA Inspection 703422 - 2010-12-21
- FDA Inspection 584834 - 2009-05-08

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christopher-s-genther/e71df42c-9adf-4a78-93e5-c364dcc06b35)
- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/d-e-hokanson-inc/30d158e6-a482-477d-954b-aab0a0900228

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7