# D E Hokanson Inc – FDA Inspection, Mar 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/d-e-hokanson-inc/ccf4406a-3387-4520-ac24-8c4b87bb5fd7
Source feed: FDA_Inspections

> FDA inspection 918525 of D E Hokanson Inc, March 19, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 918525
- Company Name: D E Hokanson Inc
- Inspection Date: 2015-03-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1040113 - 2018-02-07](https://www.keypedia.com/records/fda_inspections/d-e-hokanson-inc/e924555d-8e4f-4689-b03f-5e60c5eeb986)
- FDA Inspection 804776 - 2012-10-30
- FDA Inspection 703422 - 2010-12-21
- FDA Inspection 584834 - 2009-05-08

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